Label: AVON NUTRA EFFECTS RADIANCE DAY CREAM- octinoxate, oxybenzone, homosalate, avonbenzone cream
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Contains inactivated NDC Code(s)
NDC Code(s): 71110-0014-1 - Packager: Avon Products, Inc.
- Category: HUMAN OTC DRUG LABEL
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
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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 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, DIMETHICONE, GLYCERIN, PEG-8, CETEARYL ALCOHOL, TRISILOXANE, BEHENYL ALCOHOL, BUTYLOCTYL SALICYLATE, DILAURYL THIODIPROPIONATE, SILICA, HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, DIMETHICONE CROSSPOLYMER, CARBOMER, CETEARETH-20, THIODIPROPIONIC ACID, PHENOXYETHANOL, SODIUM HYDROXIDE, ISOHEXADECANE, CHLORPHENESIN, DISODIUM EDTA, KAEMPFERIA GALANGA ROOT EXTRACT, PARFUM/FRAGRANCE, SODIUM DEHYDROACETATE, POLYSORBATE 60, PANTHENOL, STRELITZIA NICOLAI SEED ARIL EXTRACT, TOCOPHERYL ACETATE, HELIANTHUS ANNUUS (SUNFLOWER) SEED EXTRACT, SALVIA HISPANICA SEED EXTRACT, MALTODEXTRIN, POUZOLZIA PENTANDRA EXTRACT.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AVON NUTRA EFFECTS RADIANCE DAY CREAM
octinoxate, oxybenzone, homosalate, avonbenzone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71110-0014 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 30 mg in 1 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 25 mg in 1 g OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 35 mg in 1 g Inactive Ingredients Ingredient Name Strength DILAURYL THIODIPROPIONATE (UNII: V51YH1B080) SODIUM DEHYDROACETATE (UNII: 8W46YN971G) POLYSORBATE 60 (UNII: CAL22UVI4M) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) ISOHEXADECANE (UNII: 918X1OUF1E) PANTHENOL (UNII: WV9CM0O67Z) MALTODEXTRIN (UNII: 7CVR7L4A2D) SODIUM HYDROXIDE (UNII: 55X04QC32I) DIMETHICONE (UNII: 92RU3N3Y1O) PHENOXYETHANOL (UNII: HIE492ZZ3T) CHLORPHENESIN (UNII: I670DAL4SZ) THIODIPROPIONIC ACID (UNII: 3BBK323ED8) TRISILOXANE (UNII: 9G1ZW13R0G) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71110-0014-1 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(71110-0014)
