NDC | 10096-0265-1, 10096-0265-2 |
Set ID | 94264f8c-0643-4ae5-a0f4-457f18b721a0 |
Category | HUMAN OTC DRUG LABEL |
Packager | Avon Products, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- WARNINGS
-
DOSAGE & ADMINISTRATION
Directions
• apply liberally 15 minutes before sun exposure
• children under 6 months 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, Dimethicone, Glycerin, Isododecane, HDI/Trimethylol Hexyllactone Crosspolymer, C12-15 Alkyl Benzoate, Polymethyl Methacrylate, Butylene Glycol, PEG-8, Dimethicone Crosspolymer, Trimethylsiloxysilicate, Silica, Cetyl Alcohol, Imidazolidinyl Urea, Methylparaben, Hydrogenated Lecithin,Carbomer, Disodium EDTA, Sodium Hydroxide, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aluminum Hydroxide, Alumina, Cellulose, Cetearyl Dimethicone Crosspolymer, PEG/PPG-20/23 Dimethicone, Mica/CI 77019.
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
MAGIX ILLUMINATING FACE PERFECTOR
octisalate, titanium dioxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10096-0265 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 0.9 mL in 30 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 0.657 mL in 30 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10096-0265-2 1 in 1 CARTON 1 NDC:10096-0265-1 30 mL in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 12/20/2011 Labeler - Avon Products, Inc. (001468693) Establishment Name Address ID/FEI Business Operations Avon Products, Inc. 005149471 manufacture