Label: AVON NUTRA EFFECTS HYDRATION DAY CREAM- octinoxate, homosalate, avonbenzone, oxybenzone cream
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Contains inactivated NDC Code(s)
NDC Code(s): 71110-0012-1 - Packager: Avon Products, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated June 1, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- 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 suncreen use:
Apply liberally and evenly 15 minutes before sun exposure.
Children under 6 months of age: ask a doctor.
Reapply at least every 2 hours.
Use a water-resistant sunscreen if swimming or sweating.
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-procteion measures, including:
Limite time in the sun, expecially from 10 a.m.-2 p.m.
Wear long-sleeved shirts, pants, hats and sunglasses. - STORAGE AND HANDLING
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INACTIVE INGREDIENT
Inactive ingredients
WATER/EAU, GLYCERIN, PROPANEDIOL, DIMETHICONE, HYDROGENATED POLYISOBUTENE, HYDROXYETHYL UREA, LAURYL LACTATE, CETEARYL ALCOHOL, SILICA, PEG-100 STEARATE, PENTYLENE GLYCOL, FRAGRANCE/PARFUM, PHENOXYETHANOL, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, CETEARETH-20, HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, CARBOMER, CHLORPHENESIN, DISODIUM EDTA, ISOHEXADECANE, ETHYLENE/PROPYLENE/STYRENE COPOLYMER, UREA, CHOLESTEROL, DILAURYL THIODIPROPIONATE, DIMETHICONE CROSSPOLYMER, PHYTOL, SODIUM HYDROXIDE, XANTHAN GUM, SODIUM DEHYDROACETATE, SODIUM PCA, POLYSORBATE 60, PANTHENOL, BORON NITRIDE, SODIUM HYALURONATE, TOCOPHERYL ACETATE, BUTYROSPERMUM PARKII (SHEA) BUTTER, BUTYLENE/ETHYLENE/STYRENE COPOLYMER,
HELIANTHUS ANNUUS (SUNFLOWER) SEED EXTRACT, CEREUS GRANDIFLORUS (CACTUS) FLOWER EXTRACT, SALVIA HISPANICA SEED EXTRACT, MALTODEXTRIN, POUZOLZIA PENTANDRA EXTRACT, PELVETIA CANALICULATA EXTRACT.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AVON NUTRA EFFECTS HYDRATION DAY CREAM
octinoxate, homosalate, avonbenzone, oxybenzone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71110-0012 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 55 mg in 1 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 50 mg in 1 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 29 mg in 1 g OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 10 mg in 1 g Inactive Ingredients Ingredient Name Strength DILAURYL THIODIPROPIONATE (UNII: V51YH1B080) SODIUM DEHYDROACETATE (UNII: 8W46YN971G) POLYSORBATE 60 (UNII: CAL22UVI4M) BORON NITRIDE (UNII: 2U4T60A6YD) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) PROPANEDIOL (UNII: 5965N8W85T) ISOHEXADECANE (UNII: 918X1OUF1E) CHOLESTEROL (UNII: 97C5T2UQ7J) PANTHENOL (UNII: WV9CM0O67Z) MALTODEXTRIN (UNII: 7CVR7L4A2D) PHYTOL (UNII: 5BC2RZ81NG) SODIUM HYDROXIDE (UNII: 55X04QC32I) XANTHAN GUM (UNII: TTV12P4NEE) PENTYLENE GLYCOL (UNII: 50C1307PZG) DIMETHICONE (UNII: 92RU3N3Y1O) HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR) LAURYL LACTATE (UNII: G5SU0BFK7O) PEG-100 STEARATE (UNII: YD01N1999R) PHENOXYETHANOL (UNII: HIE492ZZ3T) CHLORPHENESIN (UNII: I670DAL4SZ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71110-0012-1 1.1 g in 1 PACKET; Type 0: Not a Combination Product 03/01/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 03/01/2016 Labeler - Avon Products, Inc. (001468693) Establishment Name Address ID/FEI Business Operations Avon Manufacturing (Guangzhou) Ltd 544863277 manufacture(71110-0012)
