NDC | 71110-0016-1 |
Set ID | 6d9a615e-4491-7db1-e053-2a91aa0a600b |
Category | HUMAN OTC DRUG LABEL |
Packager | Avon Products, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
-
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, dimethicone, isododecane, butyrospermum parkii (shea) butter, caprylic/capric triglyceride, dilauryl thiodipropionate, myristyl myristate, ethylhexylglycerin, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, glyceryl stearate, peg-100 stearate, cetearyl alcohol, peg-40 stearate, isohexadecane, carbomer, phenoxyethanol, dimethiconol, ceteareth-20, silica, parfum/fragrance, disodium edta, sodium hydroxide, polysorbate 60, dimethicone crosspolymer, hydrolyzed hibiscus esculentus extract, panthenol, tocopheryl acetate, sesbania grandiflora flower extract, helianthus annuus (sunflower) seed extract, phospholipids, salvia hispanica seed extract, maltodextrin, tocopherol, pouzolzia pentandra extract, punica granatum extract, medicago sativa (alfalfa) extract.
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AVON NUTRA EFFECTS AGELESS DAY CREAM
octinoxate, oxybenzone, homosalate, avonbenzone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71110-0016 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 29 mg in 1 g OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 40 mg in 1 g Inactive Ingredients Ingredient Name Strength DILAURYL THIODIPROPIONATE (UNII: V51YH1B080) 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) PEG-100 STEARATE (UNII: YD01N1999R) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) ISODODECANE (UNII: A8289P68Y2) MYRISTYL MYRISTATE (UNII: 4042ZC00DY) PEG-40 STEARATE (UNII: ECU18C66Q7) TOCOPHEROL (UNII: R0ZB2556P8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71110-0016-1 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(71110-0016)