Label: SPF ELIO DROPS 30 GLOW- zinc oxide cream
- NDC Code(s): 62742-4233-1, 62742-4233-2
- Packager: Allure Labs Inc
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 28, 2023
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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 FOR SUNSCREEN USE: APPLY GENEROUSLY 15 MINUTES BEFORE SUN EXPOSURE. APPLY TO ALL SKIN EXPOSED BY THE SUN. 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 SUN, ESPECIALLY FROM 10 A.M. - 2 P.M. WEAR LONG-SLEEVED SHIRTS, PANTS, HATS AND SUNGLASSES. REAPPLY AT LEAST EVERY 2 HOURS. USE A WATER RESISTANT SUNSCREEN IF SWIMMING OR SWEATING IMMEDIATELY AFTER TOWEL DRYING AT LEAST EVERY 2 HOURS.
- OTHER SAFETY INFORMATION
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INACTIVE INGREDIENT
INACTIVE INGREDIENTS:ISODODECANE, SQUALANE, POLYSILICONE-11, PROPANEDIOL DICAPRYLATE/CAPRATE, CAPRYLIC/CAPRIC, TRIGLYCERIDE, POLYHYDROXYSTEARIC ACID, POLYGLYCERYL-3 POLYRICINOLEATE, TRIETHOXYCAPRYLY, SILANE, LECITHIN, HYDROGENATED PALM OIL, HYDROGENATED RAPESEED OIL, COCO-CAPRYLATE, CAPRATE, HYDRATED SILICA, ZINGIBER OFFICINALE (GINGER) ROOT EXTRACT, TOCOPHERYL ACETATE, TETRAHEXYLDECYL ASCORBATE, CAMELLIA OLEIFERA SEED OIL, POLYGLYCERYL-6 POLYRICINOLEATE, DILINOLEIC ACID/BUTANEDIOL COPOLYMER, DISODIUM STEAROYL GLUTAMATE, PRUNUS ARMENIACA, KERNEL OIL, CASTOR OIL/IPDI COPOLYMER, ALOE BARBADENESIS LEAF EXTRACT, CARTHAMUS TINCTORIUS (SAFFLOWER) SEED OIL, PISTACIA LENTISCUS (MASTIC) GUM OIL, ARGANIA SPINOSA KERNEL OIL, BISABOLOL, MAY CONTAIN +/- IRON OXIDES (CI 77492, CI 77491, CI 77499
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SPF ELIO DROPS 30 GLOW
zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62742-4233 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 15.6 g in 100 g Inactive Ingredients Ingredient Name Strength POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6) HYDROGENATED RAPESEED OIL (UNII: K168T6Y0YU) DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M) FERRIC OXIDE RED (UNII: 1K09F3G675) FERROSOFERRIC OXIDE (UNII: XM0M87F357) COCO-CAPRYLATE (UNII: 4828G836N6) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SQUALANE (UNII: GW89575KF9) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) HYDROGENATED PALM OIL (UNII: 257THB963H) SILANE (UNII: 5J076063R1) ALOE VERA LEAF (UNII: ZY81Z83H0X) SAFFLOWER OIL (UNII: 65UEH262IS) CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) DILINOLEIC ACID/BUTANEDIOL COPOLYMER (UNII: 1F2S8T535O) ISODODECANE (UNII: A8289P68Y2) CAMELLIA OIL (UNII: T1PE06G0VE) APRICOT KERNEL OIL (UNII: 54JB35T06A) CASTOR OIL (UNII: D5340Y2I9G) ARGAN OIL (UNII: 4V59G5UW9X) PISTACIA LENTISCUS RESIN OIL (UNII: ZJ39788YVA) PROPANEDIOL DICAPRYLATE/CAPRATE (UNII: F53961BX4F) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4) RED BREAST CICHLID (UNII: 492WK4ZA3B) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) POLYGLYCERYL-6 POLYRICINOLEATE (UNII: YPM0ZOC2HR) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) HYDRATED SILICA (UNII: Y6O7T4G8P9) GINGER (UNII: C5529G5JPQ) LEVOMENOL (UNII: 24WE03BX2T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62742-4233-2 1 in 1 CARTON 10/28/2023 1 NDC:62742-4233-1 29.4 g 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 Drug M020 10/28/2023 Labeler - Allure Labs Inc (926831603) Registrant - Allure Labs Inc (926831603) Establishment Name Address ID/FEI Business Operations Allure Labs Inc 926831603 manufacture(62742-4233)