NDC | 70186-564-01, 70186-566-01, 70186-567-01, 70186-568-01, 70186-569-01, 70186-570-01, 70186-571-01, 70186-572-01, 70186-573-01, 70186-574-01, 70186-575-01, 70186-576-01, 70186-577-01, 70186-578-01, 70186-579-01 |
Set ID | 0a98c31c-a57b-4368-9832-4237d4889d66 |
Category | HUMAN OTC DRUG LABEL |
Packager | Charlotte Tilbury Beauty Ltd. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- WARNINGS AND PRECAUTIONS
- ACTIVE INGREDIENT
- PURPOSE
- Uses:
- Warnings:
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
-
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), cyclopentasiloxane, cyclohexasiloxane, talc, cetyl peg/ppg-10/1 dimethicone, glycerin, nylon-12, hdi/trimethylol hexyllactone crosspolymer, acrylates/dimethicone copolymer, phenoxyethanol, benzyl alcohol, sodium chloride, magnesium sulfate, hydrogen dimethicone, sodium dehydroacetate, alumina, disteardimonium hectorite, dehydroacetic acid, potassium sorbate, benzoic acid, dimethicone, tetrasodium edta, tocopheryl acetate, aluminum hydroxide, triethoxycaprylylsilane, ascorbyl tetraisopalmitate, propylene carbonate, sodium hyaluronate, butylene glycol, silica, ethylhexylglycerin, fomes officinalis (mushroom) extract), peg-40 hydrogenated castor oil, [may contain/peut contenir (+/-): titanium dioxide (CI 77891), (iron oxides CI 77491, CI 77492, CI 77499).
- Other Information:
- Principal Display Panel - 30 mL 1.0 fl. oz.
-
INGREDIENTS AND APPEARANCE
MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70186-566 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 0.957 g in 30 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 0.282 g in 30 mL Inactive Ingredients Ingredient Name Strength 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) DIMETHICONE (UNII: 92RU3N3Y1O) 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) Product Characteristics Color brown (1 Fair) Score Shape capsule Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70186-566-01 1 in 1 CARTON 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 02/22/2016 MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70186-567 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 0.957 g in 30 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 0.282 g in 30 mL Inactive Ingredients Ingredient Name Strength 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) DIMETHICONE (UNII: 92RU3N3Y1O) 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) Product Characteristics Color brown (2 Fair) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70186-567-01 1 in 1 CARTON 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 02/22/2016 MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70186-568 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 0.957 g in 30 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 0.282 g in 30 mL Inactive Ingredients Ingredient Name Strength 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) DIMETHICONE (UNII: 92RU3N3Y1O) 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) Product Characteristics Color brown (3 Fair) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70186-568-01 1 in 1 CARTON 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 02/22/2016 MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70186-569 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 0.957 g in 30 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 0.282 g in 30 mL Inactive Ingredients Ingredient Name Strength 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) DIMETHICONE (UNII: 92RU3N3Y1O) 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) Product Characteristics Color brown (3.5 Fair) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70186-569-01 1 in 1 CARTON 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 02/22/2016 MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70186-570 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 0.957 g in 30 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 0.282 g in 30 mL Inactive Ingredients Ingredient Name Strength 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) DIMETHICONE (UNII: 92RU3N3Y1O) 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) Product Characteristics Color brown (4 Fair) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70186-570-01 1 in 1 CARTON 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 02/22/2016 MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70186-571 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 0.957 g in 30 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 0.282 g in 30 mL Inactive Ingredients Ingredient Name Strength 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) DIMETHICONE (UNII: 92RU3N3Y1O) 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) Product Characteristics Color brown (4.5 Medium) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70186-571-01 1 in 1 CARTON 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 02/22/2016 MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70186-572 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 0.957 g in 30 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 0.282 g in 30 mL Inactive Ingredients Ingredient Name Strength 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) DIMETHICONE (UNII: 92RU3N3Y1O) 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) Product Characteristics Color brown (5 Medium) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70186-572-01 1 in 1 CARTON 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 02/22/2016 MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70186-573 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 0.957 g in 30 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 0.282 g in 30 mL Inactive Ingredients Ingredient Name Strength 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) DIMETHICONE (UNII: 92RU3N3Y1O) 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) Product Characteristics Color brown (6 Medium) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70186-573-01 1 in 1 CARTON 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 02/22/2016 MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70186-574 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 0.957 g in 30 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 0.282 g in 30 mL Inactive Ingredients Ingredient Name Strength 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) DIMETHICONE (UNII: 92RU3N3Y1O) 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) Product Characteristics Color brown (7 Medium) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70186-574-01 1 in 1 CARTON 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 02/22/2016 MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70186-575 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 0.957 g in 30 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 0.282 g in 30 mL Inactive Ingredients Ingredient Name Strength 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) DIMETHICONE (UNII: 92RU3N3Y1O) 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) Product Characteristics Color brown (8 Medium) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70186-575-01 1 in 1 CARTON 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 02/22/2016 MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70186-576 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 0.957 g in 30 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 0.282 g in 30 mL Inactive Ingredients Ingredient Name Strength 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) DIMETHICONE (UNII: 92RU3N3Y1O) 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) Product Characteristics Color brown (9 Dark) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70186-576-01 1 in 1 CARTON 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 02/22/2016 MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70186-577 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 0.957 g in 30 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 0.282 g in 30 mL Inactive Ingredients Ingredient Name Strength 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) DIMETHICONE (UNII: 92RU3N3Y1O) 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) Product Characteristics Color brown (9.5 Dark) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70186-577-01 1 in 1 CARTON 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 02/22/2016 MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70186-579 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 0.957 g in 30 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 0.282 g in 30 mL Inactive Ingredients Ingredient Name Strength 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) DIMETHICONE (UNII: 92RU3N3Y1O) 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) Product Characteristics Color brown (10 Dark) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70186-579-01 1 in 1 CARTON 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 02/22/2016 MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70186-578 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 0.957 g in 30 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 0.282 g in 30 mL Inactive Ingredients Ingredient Name Strength 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) DIMETHICONE (UNII: 92RU3N3Y1O) 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) Product Characteristics Color brown (11 Dark) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70186-578-01 1 in 1 CARTON 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 02/22/2016 MAGIC FOUNDATION FLAWLESS LONG-LASTING COVERAGE SUNSCREEN BROAD SPECTRUM SPF 15
titanium dioxide and zinc oxide suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70186-564 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 0.957 g in 30 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 0.282 g in 30 mL Inactive Ingredients Ingredient Name Strength 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) DIMETHICONE (UNII: 92RU3N3Y1O) 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) Product Characteristics Color brown (12 Dark) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70186-564-01 1 in 1 CARTON 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 02/22/2016 Labeler - Charlotte Tilbury Beauty Ltd. (218353520)