Label: CLEARLY ZINQ TINTED HYDRATING FACIAL SPF GROWTH FACTOR 35- zinc oxide cream
- NDC Code(s): 62742-4259-1, 62742-4259-2
- Packager: Allure Labs
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated April 4, 2024
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
Directions •Apply generously and evenly15 minutes before sun exposure. • Reapply: • after 80 minutes of swimming or sweating • immediately after towel drying • at least every 2 hours. • 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 time in the sun, especially from 10 a.m. -2 p.m., •wear long-sleeved shirts, pants, hats and sunglasses • Children under 6 months of age: Ask a doctor.
- OTHER SAFETY INFORMATION
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INACTIVE INGREDIENT
Inactive ingredients:
Isododecane, Polysilicone-11, C13-15 Alkane, Butyloctyl Salicylate, Propanediol Dicaprylate/Caprate, Dimethicone, Polyhydroxystearic Acid, Castor oil/IPDI Copolymer, Dilinoleic Acid/Butanediol Copolymer, Disodium Stearoyl Glutamate, Polyglyceryl-6 Polyricinoleate, Polyglyceryl-3 Polyricinoleate, Triethoxycaprylylsilane, Lecithin, Coco-Caprylate/Caprate, Camellia Oleifera (Seed) Oil, Kinetin, Prunus Armeniaca (Apricot) Kernel Oil, Squalane,Aloe Barbadensis Leaf Extract, Carthamus Tinctorius (Safflower) Seed Oil, Hydrated Silica, Tocopheryl Acetate, May Contain +/-, CI 77491 (Iron Oxide), CI 77492 (Iron Oxide), CI 77499 (Iron Oxide)
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
CLEARLY ZINQ TINTED HYDRATING FACIAL SPF GROWTH FACTOR 35
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62742-4259 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 20.28 g in 100 g Inactive Ingredients Ingredient Name Strength DIMETHICONE (UNII: 92RU3N3Y1O) CASTOR OIL (UNII: D5340Y2I9G) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) C13-15 ALKANE (UNII: 114P5I43UJ) POLYGLYCERYL-6 POLYRICINOLEATE (UNII: YPM0ZOC2HR) SAFFLOWER OIL (UNII: 65UEH262IS) HYDRATED SILICA (UNII: Y6O7T4G8P9) COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) FERROSOFERRIC OXIDE (UNII: XM0M87F357) ISODODECANE (UNII: A8289P68Y2) KINETIN (UNII: P39Y9652YJ) CAMELLIA OIL (UNII: T1PE06G0VE) APRICOT KERNEL OIL (UNII: 54JB35T06A) SQUALANE (UNII: GW89575KF9) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERRIC OXIDE RED (UNII: 1K09F3G675) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) ALOE VERA LEAF (UNII: ZY81Z83H0X) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) PROPANEDIOL DICAPRYLATE/CAPRATE (UNII: F53961BX4F) DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M) POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4) DILINOLEIC ACID/BUTANEDIOL COPOLYMER (UNII: 1F2S8T535O) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62742-4259-2 1 in 1 CARTON 04/04/2024 1 NDC:62742-4259-1 48 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 04/04/2024 Labeler - Allure Labs (926831603) Registrant - Allure Labs (926831603) Establishment Name Address ID/FEI Business Operations Allure Labs 926831603 manufacture(62742-4259)