Magic Foundation Flawless Long-Lasting Coverage Sunscreen Broad Spectrum Spf 15 (Titanium Dioxide And Zinc Oxide) Suspension [Charlotte Tilbury Beauty Ltd.] -

MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15 (TITANIUM DIOXIDE AND ZINC OXIDE) SUSPENSION [CHARLOTTE TILBURY BEAUTY LTD.]
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NDC	70186-580-01, 70186-581-01, 70186-582-01, 70186-583-01, 70186-584-01, 70186-585-01, 70186-586-01, 70186-587-01, 70186-588-01, 70186-589-01, 70186-590-01, 70186-591-01, 70186-592-01, 70186-593-01, 70186-594-01, 70186-595-01, 70186-596-01, 70186-597-01, 70186-598-01, 70186-599-01
Set ID	3277c5f1-9023-4139-b38d-60c9af54cd03
Category	HUMAN OTC DRUG LABEL
Packager	Charlotte Tilbury Beauty Ltd.
Generic Name
Product Class
Product Number
Application Number	PART352

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WARNINGS AND PRECAUTIONS

Drug Facts
ACTIVE INGREDIENT
PURPOSE

Active Ingredients Purpose

Titanium Dioxide 3.19% Sunscreen
Zinc Oxide 0.94% Sunscreen
Uses:

• Helps prevent sunburn.

• If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.
Warnings:

For external use only
DO NOT USE

Do not use on damaged or broken skin.
WHEN USING

When using this product keep out of eyes. Rinse with water to remove.
STOP USE

Stop use and ask a doctor if rash occurs. water to remove.
KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.
Directions:

• Apply liberally and evenly 15 minutes before sun exposure.
• Children under 6 months of age: Ask a doctor.
• Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
- limit time in the sun, especially from 10 a.m. - 2 p.m.
- wear long-sleeved shirts, pants, hats, and sunglasses.
• Reapply at least every 2 hours or immediately after towel drying.
• Use a water-resistant sunscreen if swimming or sweating.
Inactive Ingredients:

aqua/water/eau, cyclopentasiloxane, talc, cyclohexasiloxane, cetyl peg/ppg-10/1 dimethicone, glycerin, nylon-12, hdi/trimethylol hexyllactone crosspolymer, acrylates/dimethicone copolymer, benzyl alcohol, phenoxyethanol, sodium chloride, magnesium sulfate, hydrogen dimethicone, triethoxycaprylylsilane, sodium dehydroacetate, alumina, disteardimonium hectorite, dehydroacetic acid, aluminum hydroxide, potassium sorbate, benzoic acid, tetrasodium edta, tocopheryl acetate, ascorbyl tetraisopalmitate, propylene carbonate, sodium hyaluronate, silica, butylene glycol, fomes officinalis (mushroom) extract), ethylhexylglycerin, peg-40 hydrogenated castor oil, iron oxides (CI 77491), iron oxides (CI 77492), iron oxides (CI 77499).
Other Information:

Protect the product in this container from excessive heat and direct sun.
Principal Display Panel - 30 mL 1.0 fl. oz.

Magic Foundation

Flawless Long-Lasting Coverage

Broad Spectrum Sunscreen SPF 15

30 mL 1.0 fl.oz. US

Shade 1 Fair

Shade 2 Fair

Shade 3 Fair

Shade 3.5 Fair

Shade 4 Fair

Shade 4.5 Medium

Shade 5 Medium

Shade 6 Medium

Shade 7 Medium

Shade 8 Medium

Shade 9 Dark

Shade 9.5 Dark

Shade 10 Dark

Shade 11 Dark

Shade 12 Dark

Shade O Fair

Shade 6.5 Medium

Shade 6.75 Medium

Shade 8.5 Medium

Shade 11.5 Dark

INGREDIENTS AND APPEARANCE

MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70186-586
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.693 g in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.287 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
TALC (UNII: 7SEV7J4R1U)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
GLYCERIN (UNII: PDC6A3C0OX)
NYLON-12 (UNII: 446U8J075B)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
ALUMINUM OXIDE (UNII: LMI26O6933)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
BENZOIC ACID (UNII: 8SKN0B0MIM)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
FERRIC OXIDE RED (UNII: 1K09F3G675)
HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
FERRIC OXYHYDROXIDE (UNII: 87PZU03K0K)

Product Characteristics
Color	brown (1 Fair)	Score
Shape	capsule	Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70186-586-01	1 in 1 CARTON	06/01/2018
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	06/01/2018

MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70186-587
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.693 g in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.287 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
TALC (UNII: 7SEV7J4R1U)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
GLYCERIN (UNII: PDC6A3C0OX)
NYLON-12 (UNII: 446U8J075B)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
ALUMINUM OXIDE (UNII: LMI26O6933)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
BENZOIC ACID (UNII: 8SKN0B0MIM)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
FERRIC OXIDE RED (UNII: 1K09F3G675)
HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
FERRIC OXYHYDROXIDE (UNII: 87PZU03K0K)

Product Characteristics
Color	brown (2 Fair)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70186-587-01	1 in 1 CARTON	06/01/2018
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	06/01/2018

MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70186-588
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.553 g in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.287 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
TALC (UNII: 7SEV7J4R1U)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
GLYCERIN (UNII: PDC6A3C0OX)
NYLON-12 (UNII: 446U8J075B)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
ALUMINUM OXIDE (UNII: LMI26O6933)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
BENZOIC ACID (UNII: 8SKN0B0MIM)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
FERRIC OXIDE RED (UNII: 1K09F3G675)
HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
FERRIC OXYHYDROXIDE (UNII: 87PZU03K0K)

Product Characteristics
Color	brown (3 Fair)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70186-588-01	1 in 1 CARTON	06/01/2018
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	06/01/2018

MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70186-589
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.578 g in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.287 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
TALC (UNII: 7SEV7J4R1U)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
GLYCERIN (UNII: PDC6A3C0OX)
NYLON-12 (UNII: 446U8J075B)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
ALUMINUM OXIDE (UNII: LMI26O6933)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
BENZOIC ACID (UNII: 8SKN0B0MIM)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
FERRIC OXIDE RED (UNII: 1K09F3G675)
HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
FERRIC OXYHYDROXIDE (UNII: 87PZU03K0K)

Product Characteristics
Color	brown (3.5 Fair)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70186-589-01	1 in 1 CARTON	06/01/2018
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	06/01/2018

MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70186-590
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.466 g in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.287 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
TALC (UNII: 7SEV7J4R1U)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
GLYCERIN (UNII: PDC6A3C0OX)
NYLON-12 (UNII: 446U8J075B)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
ALUMINUM OXIDE (UNII: LMI26O6933)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
BENZOIC ACID (UNII: 8SKN0B0MIM)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
FERRIC OXIDE RED (UNII: 1K09F3G675)
HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
FERRIC OXYHYDROXIDE (UNII: 87PZU03K0K)

Product Characteristics
Color	brown (4 Fair)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70186-590-01	1 in 1 CARTON	06/01/2018
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	06/01/2018

MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70186-591
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.564 g in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.287 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
TALC (UNII: 7SEV7J4R1U)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
GLYCERIN (UNII: PDC6A3C0OX)
NYLON-12 (UNII: 446U8J075B)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
ALUMINUM OXIDE (UNII: LMI26O6933)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
BENZOIC ACID (UNII: 8SKN0B0MIM)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
FERRIC OXIDE RED (UNII: 1K09F3G675)
HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
FERRIC OXYHYDROXIDE (UNII: 87PZU03K0K)

Product Characteristics
Color	brown (4.5 Medium)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70186-591-01	1 in 1 CARTON	06/01/2018
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	06/01/2018

MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70186-592
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.4208 g in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.287 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
TALC (UNII: 7SEV7J4R1U)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
GLYCERIN (UNII: PDC6A3C0OX)
NYLON-12 (UNII: 446U8J075B)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
ALUMINUM OXIDE (UNII: LMI26O6933)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
BENZOIC ACID (UNII: 8SKN0B0MIM)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
FERRIC OXIDE RED (UNII: 1K09F3G675)
HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
FERRIC OXYHYDROXIDE (UNII: 87PZU03K0K)

Product Characteristics
Color	brown (5 Medium)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70186-592-01	1 in 1 CARTON	06/01/2018
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	06/01/2018

MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70186-593
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.469 g in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.287 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
TALC (UNII: 7SEV7J4R1U)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
GLYCERIN (UNII: PDC6A3C0OX)
NYLON-12 (UNII: 446U8J075B)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
ALUMINUM OXIDE (UNII: LMI26O6933)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
BENZOIC ACID (UNII: 8SKN0B0MIM)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
FERRIC OXIDE RED (UNII: 1K09F3G675)
HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
FERRIC OXYHYDROXIDE (UNII: 87PZU03K0K)

Product Characteristics
Color	brown (6 Medium)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70186-593-01	1 in 1 CARTON	06/01/2018
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	06/01/2018

MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70186-594
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.193 g in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.287 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
TALC (UNII: 7SEV7J4R1U)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
GLYCERIN (UNII: PDC6A3C0OX)
NYLON-12 (UNII: 446U8J075B)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
ALUMINUM OXIDE (UNII: LMI26O6933)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
BENZOIC ACID (UNII: 8SKN0B0MIM)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
FERRIC OXIDE RED (UNII: 1K09F3G675)
HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
FERRIC OXYHYDROXIDE (UNII: 87PZU03K0K)

Product Characteristics
Color	brown (7 Medium)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70186-594-01	1 in 1 CARTON	06/01/2018
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	06/01/2018

MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70186-595
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.111 g in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.287 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
TALC (UNII: 7SEV7J4R1U)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
GLYCERIN (UNII: PDC6A3C0OX)
NYLON-12 (UNII: 446U8J075B)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
ALUMINUM OXIDE (UNII: LMI26O6933)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
BENZOIC ACID (UNII: 8SKN0B0MIM)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
FERRIC OXIDE RED (UNII: 1K09F3G675)
HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
FERRIC OXYHYDROXIDE (UNII: 87PZU03K0K)

Product Characteristics
Color	brown (8 Medium)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70186-595-01	1 in 1 CARTON	06/01/2018
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	06/01/2018

MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70186-596
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1.572 g in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.287 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
TALC (UNII: 7SEV7J4R1U)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
GLYCERIN (UNII: PDC6A3C0OX)
NYLON-12 (UNII: 446U8J075B)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
ALUMINUM OXIDE (UNII: LMI26O6933)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
BENZOIC ACID (UNII: 8SKN0B0MIM)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
FERRIC OXIDE RED (UNII: 1K09F3G675)
HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
FERRIC OXYHYDROXIDE (UNII: 87PZU03K0K)

Product Characteristics
Color	brown (9 Dark)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70186-596-01	1 in 1 CARTON	06/01/2018
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	06/01/2018

MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70186-597
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1.502 g in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.287 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
TALC (UNII: 7SEV7J4R1U)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
GLYCERIN (UNII: PDC6A3C0OX)
NYLON-12 (UNII: 446U8J075B)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
ALUMINUM OXIDE (UNII: LMI26O6933)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
BENZOIC ACID (UNII: 8SKN0B0MIM)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
FERRIC OXIDE RED (UNII: 1K09F3G675)
HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
FERRIC OXYHYDROXIDE (UNII: 87PZU03K0K)

Product Characteristics
Color	brown (9.5 Dark)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70186-597-01	1 in 1 CARTON	06/01/2018
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	06/01/2018

MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70186-599
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1.058 g in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.287 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
TALC (UNII: 7SEV7J4R1U)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
GLYCERIN (UNII: PDC6A3C0OX)
NYLON-12 (UNII: 446U8J075B)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
ALUMINUM OXIDE (UNII: LMI26O6933)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
BENZOIC ACID (UNII: 8SKN0B0MIM)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
FERRIC OXIDE RED (UNII: 1K09F3G675)
HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
FERRIC OXYHYDROXIDE (UNII: 87PZU03K0K)

Product Characteristics
Color	brown (10 Dark)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70186-599-01	1 in 1 CARTON	06/01/2018
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	06/01/2018

MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70186-598
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1.058 g in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.287 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
TALC (UNII: 7SEV7J4R1U)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
GLYCERIN (UNII: PDC6A3C0OX)
NYLON-12 (UNII: 446U8J075B)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
ALUMINUM OXIDE (UNII: LMI26O6933)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
BENZOIC ACID (UNII: 8SKN0B0MIM)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
FERRIC OXIDE RED (UNII: 1K09F3G675)
HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
FERRIC OXYHYDROXIDE (UNII: 87PZU03K0K)

Product Characteristics
Color	brown (11 Dark)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70186-598-01	1 in 1 CARTON	06/01/2018
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	06/01/2018

MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70186-585
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1.058 g in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.287 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
TALC (UNII: 7SEV7J4R1U)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
GLYCERIN (UNII: PDC6A3C0OX)
NYLON-12 (UNII: 446U8J075B)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
ALUMINUM OXIDE (UNII: LMI26O6933)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
BENZOIC ACID (UNII: 8SKN0B0MIM)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
FERRIC OXIDE RED (UNII: 1K09F3G675)
HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
FERRIC OXYHYDROXIDE (UNII: 87PZU03K0K)

Product Characteristics
Color	brown (12 Dark)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70186-585-01	1 in 1 CARTON	06/01/2018
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	06/01/2018

MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70186-580
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.693 g in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.287 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
TALC (UNII: 7SEV7J4R1U)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
GLYCERIN (UNII: PDC6A3C0OX)
NYLON-12 (UNII: 446U8J075B)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
ALUMINUM OXIDE (UNII: LMI26O6933)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
BENZOIC ACID (UNII: 8SKN0B0MIM)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
FERRIC OXIDE RED (UNII: 1K09F3G675)
HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
FERRIC OXYHYDROXIDE (UNII: 87PZU03K0K)

Product Characteristics
Color	brown (0 Fair)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70186-580-01	1 in 1 CARTON	06/01/2018
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	06/01/2018

MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70186-581
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.401 g in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.287 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
TALC (UNII: 7SEV7J4R1U)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
GLYCERIN (UNII: PDC6A3C0OX)
NYLON-12 (UNII: 446U8J075B)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
ALUMINUM OXIDE (UNII: LMI26O6933)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
BENZOIC ACID (UNII: 8SKN0B0MIM)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
FERRIC OXIDE RED (UNII: 1K09F3G675)
HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
FERRIC OXYHYDROXIDE (UNII: 87PZU03K0K)

Product Characteristics
Color	brown (6.5 Medium)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70186-581-01	1 in 1 CARTON	06/01/2018
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	06/01/2018

MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70186-582
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	2.394 g in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.287 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
TALC (UNII: 7SEV7J4R1U)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
GLYCERIN (UNII: PDC6A3C0OX)
NYLON-12 (UNII: 446U8J075B)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
ALUMINUM OXIDE (UNII: LMI26O6933)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
BENZOIC ACID (UNII: 8SKN0B0MIM)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
FERRIC OXIDE RED (UNII: 1K09F3G675)
HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
FERRIC OXYHYDROXIDE (UNII: 87PZU03K0K)

Product Characteristics
Color	brown (6.75 Medium)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70186-582-01	1 in 1 CARTON	06/01/2018
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	06/01/2018

MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70186-583
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1.830 g in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.287 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
TALC (UNII: 7SEV7J4R1U)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
GLYCERIN (UNII: PDC6A3C0OX)
NYLON-12 (UNII: 446U8J075B)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
ALUMINUM OXIDE (UNII: LMI26O6933)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
BENZOIC ACID (UNII: 8SKN0B0MIM)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
FERRIC OXIDE RED (UNII: 1K09F3G675)
HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
FERRIC OXYHYDROXIDE (UNII: 87PZU03K0K)

Product Characteristics
Color	brown (8.5 Medium)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70186-583-01	1 in 1 CARTON	06/01/2018
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	06/01/2018

MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspension

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70186-584
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1.058 g in 30 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.287 g in 30 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
TALC (UNII: 7SEV7J4R1U)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X)
GLYCERIN (UNII: PDC6A3C0OX)
NYLON-12 (UNII: 446U8J075B)
HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
ALUMINUM OXIDE (UNII: LMI26O6933)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
BENZOIC ACID (UNII: 8SKN0B0MIM)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
LARICIFOMES OFFICINALIS FRUITING BODY (UNII: 7IFM8431X3)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
FERRIC OXIDE RED (UNII: 1K09F3G675)
HYDROGEN DIMETHICONE (20 CST) (UNII: 12Z59IF64N)
FERRIC OXYHYDROXIDE (UNII: 87PZU03K0K)

Product Characteristics
Color	brown (11.5 Dark)	Score
Shape		Size
Flavor		Imprint Code
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:70186-584-01	1 in 1 CARTON	06/01/2018
1		30 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	06/01/2018

Labeler - Charlotte Tilbury Beauty Ltd. (218353520)

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Medic

MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15 (TITANIUM DIOXIDE AND ZINC OXIDE) SUSPENSION [CHARLOTTE TILBURY BEAUTY LTD.]

Shade 1 Fair

Shade 2 Fair

Shade 3 Fair

Shade 3.5 Fair

Shade 4 Fair

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