Label: AVON ELEMENTS MOISTURE BOOST DAILY MOISTURE- octinoxate, octisalate, avobenzone lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 10096-0301-1, 10096-0301-2, 10096-0301-3 - Packager: New Avon LLC
- 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 February 19, 2016
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- WARNINGS
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DOSAGE & ADMINISTRATION
Directions
- apply generously and evenly over cleansed, dry skin on face and neck 15 minutes before sun exposure
- children under 6 month of age:ask a doctor
- reapply at least every 2 hours
- use a water resistant sunscreen if swimming or sweating
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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
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INACTIVE INGREDIENT
Inactive ingredients:
water/eau, glycerin, propanediol, cyclopentasiloxane, hydrogenated polyisobutene, hydroxyethyl urea, dimethicone, saccharomyces/ zinc ferment, cereus grandiflorus (cactus) flower extract, pelvetia canaliculata extract, butyrospermum parkii (shea) butter, sodium hyaluronate, tocopheryl acetate, sodium PCA, urea, phytol, lauryl lactate, silica, PEG-100 stearate, pentylene glycol, phenoxyethanol, acrylates/C10-30 alkyl acrylate crosspolymer, hydroxyethyl acrylate/ sodium acryloyldimethyl taurate copolymer, carbomer, chlorphenesin, disodium EDTA, isohexadecane, sodium hydroxide, ethylene/propylene/styrene copolymer, cetyl alcohol, cholesterol, dimethicone crosspolymer, dilauryl thiodipropionate, xanthan gum, sodium dehydroacetate, polysorbate 60, boron nitride, butylene/ethylene/styrene copolymer, parfum/fragrance. - QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AVON ELEMENTS MOISTURE BOOST DAILY MOISTURE
octinoxate, octisalate, avobenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10096-0301 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 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 47.5 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 28.5 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10096-0301-2 1 in 1 CARTON 1 NDC:10096-0301-1 118 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 2 NDC:10096-0301-3 1.1 mL in 1 PACKET; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 04/01/2013 Labeler - New Avon LLC (080143520) Establishment Name Address ID/FEI Business Operations Avon Products, Inc 005149471 manufacture(10096-0301)
