Label: SOLUTIONS A.M. TOTAL RADIANCE- octinoxate, octisalate, avobenzone lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 10096-0168-1, 10096-0168-2, 10096-0168-3 - Packager: Avon Products, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated February 8, 2013
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- ACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
- WARNINGS
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
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INACTIVE INGREDIENT
Inactive ingredients
Water, Butylene Glycol, Glycerin, Cyclopentasiloxane, Hydrogenated Polyisobutene, Hydroxyethyl Urea, Dimethicone, Lauryl Lactate, Dilauryl Thiodipropionate, Calcium PCA, Lactoferrin, Palmitoyl Oligopeptide, Saccharomyces Ferment Filtrate, Saccharomyces Lysate Extract, Phospholipids, Phytol, Tocopheryl Acetate, Aframomum Melegueta Seed Extract, Butyrospermum Parkii (Shea Butter), Ceramide 2, Cholesterol, DNA, Foeniculum Vulgare (Fennel) Seed Extract, Viola Tricolor Extract, Yeast Extract, PEG-10 Rapeseed Sterol, Urea, Caprylic/Capric Triglyceride, C12-15 Alkyl Benzoate, PEG-100 Stearate, Pentylene Glycol, Hexylene Glycol, Caprylyl Glycol, Boron Nitride, Silica, Isohexadecane, Cetyl Alcohol, Dimethiconol, Tribehenin, Polysorbate 60, Sorbitan Isostearate, Xanthan Gum, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Butylene/Ethylene/Styrene Copolymer, Ethylene/Propylene/Styrene Copolymer, Dimethicone Crosspolymer, Fragrance, Carbomer, Sodium Dehydroacetate, Chlorphenesin, Disodium EDTA, Phenoxyethanol, Sodium Hydroxide. - QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SOLUTIONS A.M. TOTAL RADIANCE
octinoxate, octisalate, avobenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10096-0168 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 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:10096-0168-2 1 in 1 CARTON 1 NDC:10096-0168-1 118 mL in 1 BOTTLE, PUMP 2 NDC:10096-0168-3 1.1 mL in 1 PACKAGE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 02/08/2013 Labeler - Avon Products, Inc (001468693) Establishment Name Address ID/FEI Business Operations Avon Products, Inc 005149471 manufacture(10096-0168)