Label: SKIN 79 SUPER PLUS BEBLESH BALM SPF25 PA (40G)- titanium dioxide, zinc oxide cream
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Contains inactivated NDC Code(s)
NDC Code(s): 49715-002-01 - Packager: WIZCOZ CORPORATION LTD
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 November 9, 2009
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- PRINCIPAL DISPLAY PANEL
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ACTIVE INGREDIENT
INGREDIENTS:
Water, Propylene Glycol, Cyclomethicone, Dimethicone, Titanium Dioxide, Isopropyl Palmitate, Talc, Ethylhexyl Methoxycinnamate, Butylene Glycol, Dicaprylate/Dicaprate, Prunus Amygdalus Delcis (Sweet Almond) Oil, Ethylhexyl Salicylate, Digenlacrythrityl Hexahydroxystearate/Hexastearate/Hexarosinate, Cetyl PEG/PPG-10/1 Dimethicone, Arbulia, Zinc Oxide, Polyglyceryl-4 Isostearate, Magnesium Sulfate, Dimethicone[Vinyl] Dimethicone Crosspolymer, Iron Oxides, Silica, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Portulaca Oleracea Extract, Piper Methyslicum Leaf/Root/Steam Extract, Phenoxyethanol, Trihydroxystearia, Disteardimonium Hectorite, Glycosyl Trichalose, Aluminum Hydroxide, Aluminum Stearate, Methylparaben, Hydrogenated Starch Hydrolysate, Methicone, Tocopheryl Acetate, Propylparaben, Fragrance, Hydrogenated Lecithin, Citrus Umshiu Fruit Oil, Cholesterol, Ceramide 3, Nelumbo Nucifera Flower Water, Medocassoside, Caviar Extract, Camellia Sipcasis Leaf Extract, Aloe Barbedensis Leaf Juice, Lycium Chinenese Fruit Extract, Hellanthus Annus (Sun Flower) Extract, Schizandra Chinensis Fruit Extract, Hedera Helix (Ivy) Extract, Cornus Officixalis Fruit Extract, Bubylparaben, Glycerin, Adenosine, Caprylic/capric Triglyceride, Triclosan, Phytic Acid, Ubiquinose, BHT, Gold
- WHEN USING
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INGREDIENTS AND APPEARANCE
SKIN 79 SUPER PLUS BEBLESH BALM SPF25 PA (40G)
titanium dioxide, zinc oxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49715-002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM - UNII:D1JT611TNE) TITANIUM DIOXIDE 1.92 g in 40 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC - UNII:J41CSQ7QDS) ZINC OXIDE 0.78 g in 40 g Inactive Ingredients Ingredient Name Strength DIMETHICONE (UNII: 92RU3N3Y1O) 2.2 g in 40 g ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) 0.072 g in 40 g Product Characteristics Color brown (Color is Beige) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49715-002-01 40 g in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 12/01/2009 Labeler - WIZCOZ CORPORATION LTD (690397273) Registrant - WIZCOZ CORPORATION LTD (690397273) Establishment Name Address ID/FEI Business Operations WIZCOZ CORPORATION LTD 690397273 manufacture
