NDC | 10096-0144-1, 10096-0144-2 |
Set ID | c13846a9-3af3-41aa-9185-c5e0bfbc2fe8 |
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, Butylene Glycol, Glycerin, PEG-8, Dimethicone, Nylon-12, Citrus Medica Limonum (Lemon) Fruit Extract, Pyrus Malus (Apple) Fruit Extract, Fumaria Officinalis Flower/Leaf/Stem Extract, Epilobium Angustifolium Flower/Leaf/Stem Extract, Vanilla Planifolia Fruit Extract, Theobroma Cacao (Cocoa) Extract, Vaccinium Angustifolium (Blueberry) Fruit Extract, Rubus Idaeus (Raspberry) Fruit Extract, Rubus Fruticosus (Blackberry) Fruit Extract, Vitis Vinifera (Grape) Fruit Extract, Tromethamine, Silica, Trimethylsiloxysilicate, Glyceryl Stearate, Hydrogenated Lecithin, Carbomer, Polyglyceryl-3 Diisostearate, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Squalane, Dimethicone/Vinyl Dimethicone Crosspolymer, Caprylic/Capric Triglyceride, Fumaric Acid, Citric Acid, Disodium EDTA, Benzyl Alcohol, Cetyl Alcohol, Polysorbate 60, Methylparaben, Propylparaben
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
MARK. FOR GOONESS FACE ANTIOXIDANT SKIN MOISTURIZING
homosalate, octinoxate, octisalate, oxybenzone, avobenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10096-0144 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 50 mg in 1 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 50 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:10096-0144-2 1 in 1 CARTON 1 NDC:10096-0144-1 50 mL in 1 JAR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 03/08/2013 Labeler - Avon Products, Inc. (001468693) Establishment Name Address ID/FEI Business Operations Avon Products, Inc. 005149471 manufacture(10096-0144)