NDC | 10096-0318-1, 10096-0318-2, 10096-0318-3 |
Set ID | 9aa667d8-3c67-4641-b9f8-31c82fa21891 |
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
For sunscreen use:
- 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, glycerin, dimethicone, PEG-8, trisiloxane, ethylhexyl isononanoate, HDI/trimethylol hexyllactone crosspolymer, cetyl alcohol, caprylyl glycol, behenyl alcohol, carbomer, dilauryl thiodipropionate, galactoarabinan, parfum/fragrance, phytol, thiodipropionic
acid, sodium hydroxide, glyceryl stearate, phenoxyethanol, trimethylsiloxysilicate, hydrogenated lecithin, acrylates/C10-30 alkyl acrylate crosspolymer, disodium EDTA, polyglyceryl-3 diisostearate, choleth-24, hexylene glycol, tocopherol, ceteth-24, panthenol, silica, tocopheryl
acetate, sesbania grandiflora flower extract, amethyst extract, phospholipids, pueraria lobata symbiosome extract, saccharomyces/calcium ferment, zea mays (corn) kernel extract, sphingolipids, saccharomyces/copper ferment, saccharomyces/potassium ferment, saccharomyces/magnesium ferment, saccharomyces/zinc ferment, saccharomyces/manganese ferment, saccharomyces/iron ferment, saccharomyces/silicon ferment. - QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
AVON ELEMENTS YOUTH RESTORING MULTI-PURPOSE
homosalate, octinoxate, oxybenzone, avobenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10096-0318 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 80 mg in 1 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 50 mg in 1 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 40 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 29 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10096-0318-2 1 in 1 CARTON 1 NDC:10096-0318-1 50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 2 NDC:10096-0318-3 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 03/17/2014 Labeler - New Avon LLC (080143520) Establishment Name Address ID/FEI Business Operations Avon Products, Inc 005149471 manufacture(10096-0318)