NDC | 10096-0314-1 |
Set ID | c224c9dc-e218-4a0c-8e6c-a3b9c473bcab |
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 months of age: ask a doctor
• reapply after 80 minutes of swimming or sweating
• immediately after towel drying• at least every 2 hours
• 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, dimethicone, butylene glycol, glycerin, PEG-8, SD alcohol 40-B, ethylhexyl isononanoate, cetyl alcohol, triethanolamine, menthyl PCA, parfum/fragrance, phenoxyethanol, glyceryl stearate, trimethylsiloxysilicate, hydrogenated lecithin, carbomer, acrylates/C10-30 alkyl acrylate crosspolymer, chlorphenesin, disodium EDTA, polyglyceryl-3 diisostearate, kaempferia galanga root extract, dimethicone/vinyl dimethicone crosspolymer, menthol, panthenol, silica, sodium dehydroacetate, phytol, lupinus luteus seed extract, triticum vulgare (wheat) germ extract, prunus amygdalus dulcis (sweet almond) fruit extract, linum usitatissimum (linseed) seed extract. - QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
AVON SUN SPORT REFRESH SUNSCREEN
homosalate, octinoxate, octisalate, oxybenzone, avobenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10096-0314 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 75 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 47.5 mg in 1 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 45 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10096-0314-1 236 mL in 1 TUBE; 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 12/12/2013 Labeler - New Avon LLC (080143520) Establishment Name Address ID/FEI Business Operations Avon Products, Inc 005149471 manufacture(10096-0314)