NDC | 10096-0299-1, 10096-0299-2, 10096-0299-3 |
Set ID | c68bfac8-f921-4b07-85b1-d522a17584b0 |
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 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, butylene glycol, cetearyl alcohol, isononyl isononanoate, dimethicone, silica, dilauryl thiodipropionate, saccharomyces/calcium
ferment, amethyst extract, glycine soja (soybean) seed extract, daucus carota sativa (carrot) root extract, saccharomyces/copper ferment,
saccharomyces ferment lysate filtrate, saccharomyces/magnesium ferment, saccharomyces/potassium ferment, saccharomyces/zinc
ferment, saccharomyces/manganese ferment, palmitoyl oligopeptide, palmitoyl tetrapeptide-7, saccharomyces/iron ferment, saccharomyces/silicon ferment, kaempferia galanga root extract, parfum/fragrance, polymethylsilsesquioxane, trisiloxane, cetearyl glucoside, phenoxyethanol, choleth-24, glycerin, ceteth-24, ceteareth-20, caprylyl glycol, xanthan gum, carbomer, disodium EDTA, acrylates/C10-30 alkyl acrylate crosspolymer, sodium hydroxide, mica/CI 77019, titanium dioxide/CI 77891. - QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
AVON ELEMENTS YOUTH-RESTORING ANTI-WRINKLE MOISTURE
octinoxate, octisalate, oxybenzone, avobenzone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10096-0299 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 71.2 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 47.5 mg in 1 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 20 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 20 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10096-0299-2 1 in 1 CARTON 1 NDC:10096-0299-1 50 mL in 1 JAR; Type 0: Not a Combination Product 2 NDC:10096-0299-3 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(10096-0299)