Label: AVON ANEW PLATINUM DAY-CREAM SPF 25 SUNSCREEN- avobenzone, octinoxate, octisalate, oxybenzone cream
- NDC Code(s): 10096-2550-1
- Packager: The Avon Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 3, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Purpose
- Uses
- Warnings
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Directions
For sunscreen use:
- apply liberally 15 minutes before sun exposure
- children less than 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 protection measures including:- limit time in the sun, especially from 10 a.m. – 2 p.m.
- wear long-sleeved shirts, pants, hats, and sunglasses
- STORAGE AND HANDLING
- Other information
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Inactive Ingredients:
WATER, GLYCERIN, SILICA, DIMETHICONE, STEARIC ACID, STEARYL ALCOHOL, NONENOL, SAPINDUS RARAK FRUIT EXTRACT, POUZOLZIA PENTANDRA EXTRACT, METHOXYBENZOYL METHYLSULFONYL OXOPIPERIDINYL PIPERAZINECARBOXAMIDE, THIAZOLYLALANINE, TRISILOXANE, DIMETHICONOL, MYRISTYL MYRISTATE, MALTODEXTRIN, PEG-100 STEARATE, CAPRYLYL GLYCOL, GLYCERYL STEARATE, SODIUM POLYACRYLATE, POLYURETHANE-40, POTASSIUM HYDROXIDE, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, DISODIUM EDTA, 1,2-HEXANEDIOL, FRAGRANCE
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Principal Display Panel:
AVON
ANEW
PLATINUM
DAY CREAM
BROAD SPECTRUM SPF 25
SUNSCREEN
DAY
50 g/net wt. 1.7 oz.
This daily moisturizer helps define and resculpt the
look of sagging skin for a more youthful appearance.
Provides UVA/UVB protection.
To order, contact your Avon Independent Sales Representative or call:
1-800-FOR-AVON www.avon.com
ASSEMBLED IN USA
DISTR. THE AVON COMPANY, NEW YORK, NY 10006
©2023 THE AVON COMPANY C226708
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INGREDIENTS AND APPEARANCE
AVON ANEW PLATINUM DAY-CREAM SPF 25 SUNSCREEN
avobenzone, octinoxate, octisalate, oxybenzone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10096-2550 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 7.5 mg in 1 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 4.75 mg in 1 g OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 4 mg in 1 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 2.85 mg in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10096-2550-1 50 g in 1 JAR; Type 0: Not a Combination Product 01/03/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/03/2024 Labeler - The Avon Company (080143520) Establishment Name Address ID/FEI Business Operations Cosmax Usa, Corporation 010990210 manufacture(10096-2550)