NDC | 62742-4088-1, 62742-4088-2 |
Set ID | 5b6c0b4f-7d1a-49bf-bff3-c150698ccc26 |
Category | HUMAN OTC DRUG LABEL |
Packager | Allure Labs Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS AND PRECAUTIONS
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
-
DOSAGE & ADMINISTRATION
For Sunscreen use:
- Apply liberally 15 minutes before sun exposer.
- Use a water resistant sunscreen if swimming or sweating.
- Reapply at least every 2 hours.
- Children under 6 months: ask a doctor.
- Sun protection measures.Spending time in the sun increase your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with a Broad Spectrum SPF 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 sleeve shirts, pants, hats and sunglasses.
-
INACTIVE INGREDIENT
Water, Cyclopentasiloxane, C12-15 Alkyl Benzoate, Dimethicone Ployglyceryl-3, Polydimethylsiloxyethyl Dimethicone, Dimethicone/PEG -10/15 Crosspolymer, Stearic Acid, Aluminum Hydroxide, Sodium Chloride, Glycerin, Magnolia officinallis Bark Extract, Ectoin, Caprylyl Glycol, Teprenone, Sodium Hyaluronate, Vitis Vinifera, (Grape) seed extract, Tetrahexyldecyl Ascorbate, Ergothioneine, Tocopheryl Acetate, Tocopherol, Maltodextrin, Lecithin, Ethylhexyl Palmitate Caprylyc/Capric Triglyceride, PEG/PPG-18/18 Dimethicone, Polyglycerin-3 Crosspolymer, Hexyl Laurate, Cyclohexasiloxane, Triethoxysilylethyl Polydimethylsiloxyethyl Hexyl Dimethicone, Dimethicone/Venyl Dimethicone Crosspolymer, Polyglyceryl-4 Isostearate, Cetyl PEG/PPG-10/1 Dimethicone, Silica Dimethyl Sylilate, Triethoxycaprylylsilane, Phenoxyethanol, Ethylhexylglycerin, Butylene Glycol, Hexylene Glycol Fragrance, Mica, Silaca, May contains: Iron Oxide.
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
EXTRA LIGHT TINTED RADIANCE MOISTURIZER BROAD SPECTRUM SPF 32
zinc oxide and titanium dioxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62742-4088 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 60 mg in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 45 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) DIMETHICONE (UNII: 92RU3N3Y1O) STEARIC ACID (UNII: 4ELV7Z65AP) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) SODIUM CHLORIDE (UNII: 451W47IQ8X) GLYCERIN (UNII: PDC6A3C0OX) MAGNOLIA OFFICINALIS BARK (UNII: 5M609NV974) ECTOINE (UNII: 7GXZ3858RY) CAPRYLYL GLYCOL (UNII: 00YIU5438U) TEPRENONE (UNII: S8S8451A4O) HYALURONATE SODIUM (UNII: YSE9PPT4TH) VITIS VINIFERA SEED (UNII: C34U15ICXA) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) ERGOTHIONEINE (UNII: BDZ3DQM98W) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TOCOPHEROL (UNII: R0ZB2556P8) MALTODEXTRIN (UNII: 7CVR7L4A2D) EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV) ETHYLHEXYL PALMITATE (UNII: 2865993309) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794) HEXYL LAURATE (UNII: 4CG9F9W01Q) CYCLOMETHICONE 6 (UNII: XHK3U310BA) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X) SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) HEXYLENE GLYCOL (UNII: KEH0A3F75J) MICA (UNII: V8A1AW0880) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62742-4088-2 1 in 1 CARTON 05/24/2017 1 NDC:62742-4088-1 30 mL in 1 TUBE; 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 05/24/2017 Labeler - Allure Labs Inc. (926831603)