NDC | 10096-0301-1, 10096-0301-2, 10096-0301-3 |
Set ID | 6c2e6fbf-f3ae-42c3-bd73-a0c95527df5e |
Category | HUMAN OTC DRUG LABEL |
Packager | New Avon LLC |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- WARNINGS
-
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
-
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
-
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
-
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)