Label: SKIN 79 SUPER PLUS BEBLESH BALM TRIPLE FUNCTIONS SPF25 PA (40G)- zinc oxide, octisalate, titanium dioxide cream
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Contains inactivated NDC Code(s)
NDC Code(s): 49715-005-01 - 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 DIACIS (SWEET ALMOND) OIL, ETHYLHEXYL SALICYLATE, DIPENTAERYTHRITYL HEXAHYDROXYSTEARATE/HEXASTEARATE/HEXAROSINATE, CETYL PEG/PPG-10/1 DIMETHICONE, ARBUTIN, ZINC OXIDE, POLYGLYCERYL-4 ISOSTEARATE, MAGNESIUM SULFATE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, IRON OXIDES, SILICA, VINYL DIMETHICONE/METHICONE SISSESQUIOXANE CROSSPOLYER, PORTULACA OLERACEA EXTRACT, PIPER METHYSTICUM LEAF/ROOT/STEM EXTRACT, PHENOSYETHANOL, TRIHYDROXYSTEARIN, DISTEARDIMONIUM HECTORITE, GLYCOSYL TREMALOSE, ALUMINUM HYDROXIDE, ALUMINUM STEARATE, METHYLPARABEN, HYDROGENATED STARCH HYDROLYSATE, METHICONE, TOCOPHEYL ACETATE, HYDROGENATED LECITHIN, NELUMBO NUCIFERA FLOWER WATER, MADECASSOSIDE, CAMELLIA SINENSIS LEAF EXTRACT, ALOE BARBEDENSIS LEAF JUICE, CHOLESTEROL, CERAMIDE 3, LYCIUM CHINENSE FRUTI EXTRACT, HELIANTHUS ANNUUS (SUNFLOWER) EXTRACT, SCHIZANDRA CHINENSIS FRUIT EXTRACT, HEDERA HELIX (IVY) EXTRACT, CORNUS OFFICINALIS FRUIT EXTRACT, FRAGRANCE, PROPYLPARABEN, BUTYLPARABEN, GLYCERIN, ADENOSINE, CAPRYLIC/CAPRIC TRIGLYCERIDE, TRICLOSAN, PHYTIC ACID, UBIQUINONE, BHT
- WHEN USING
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INGREDIENTS AND APPEARANCE
SKIN 79 SUPER PLUS BEBLESH BALM TRIPLE FUNCTIONS SPF25 PA (40G)
zinc oxide, octisalate, titanium dioxide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49715-005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC - UNII:J41CSQ7QDS) ZINC OXIDE 0.78 g in 40 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 0.8 g in 40 g OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 1.2 g in 40 g TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM - UNII:D1JT611TNE) TITANIUM DIOXIDE 1.92 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:49715-005-01 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
