Label: SKIN79 SUPER PLUS BEBLESH BALM TRIPLE FUNCTIONS SPF25 PA (5G)- zinc oxide, octisalate, octinoxate, titanium dioxide cream

  • 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

    BOX LABEL

  • ACTIVE INGREDIENT



    INGREDIENTS:

    WATER, PROPYLENE GLYCOL, CYCLOMETHICONE, DIMETHICONE, TITANIUM DIOXIDE, ISOPROPYL PALMITATE, TALC, ETHYLHEXYL METHOXYCINNAMATE, BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE, PRUNUS AMYGDALUS DIACIA (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 SILSESQUIOXANE CROSSPOLYER, PORTULACA OLERACEA EXTRACT, PIPER METHYSTICUM LEAF/ROOT/STEM EXTRACT, PHENOXYETHANOL, TRIHYDROXYSTEARIN, DISTEARDIMONIUM HECTORITE, GLYCOSYL TREMALOSE, ALUMINUM HYDROXIDE, ALUMINUM STEARATE, METHYLPARABEN, HYDROGENATED STARCH HYDROLYSATE, METHICONE, TOCOPHERYL ACETATE, HYDROGENATED LECITHIN, NELUMBO NUCIFERA FLOWER WATER, MADECASSOSIDE, CAMELLA SINENSIS LEAF EXTRACT, ALOE BARBEDENSIS LEAF JUICE, CHOLESTEROL, CERAMIDE 3, LYCIUM CHINENSE FRUIT EXTRACT, HELIANTHUS ANNUUS (SUNFLOWER) EXTRACT, SCHIZANDRA CHINENSIS FRUIT EXTRACT, HEDERA HELIX (IVY) EXTRACT, CORNUS OFFICINALIS FRUTI EXTRACT, FRAGRANCE, PROPYLPARABEN, BUTYLPARABEN, GLYCERIN, ADENOSINE, CAPRYLIC/CAPRIC TRIGLYCERIDE, TRICLOSAN, PHYTIC ACID, UBIQUNONE, BHT

  • WHEN USING



    DIRECTIONS:

    Use it proper quantity on the area of your face like patting at the last step of skin care.

  • INGREDIENTS AND APPEARANCE
    SKIN79 SUPER PLUS BEBLESH BALM TRIPLE FUNCTIONS SPF25 PA (5G) 
    zinc oxide, octisalate, octinoxate, titanium dioxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49715-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC - UNII:J41CSQ7QDS) ZINC OXIDE0.1 g  in 5 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE0.1 g  in 5 g
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE0.15 g  in 5 g
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM - UNII:D1JT611TNE) TITANIUM DIOXIDE0.24 g  in 5 g
    Inactive Ingredients
    Ingredient NameStrength
    DIMETHICONE (UNII: 92RU3N3Y1O) 0.275 g  in 5 g
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) 0.009 g  in 5 g
    Product Characteristics
    Colorbrown (Color is Beige) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49715-003-035 g in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35210/01/2009
    Labeler - WIZCOZ CORPORATION LTD (690397273)
    Registrant - WIZCOZ CORPORATION LTD (690397273)
    Establishment
    NameAddressID/FEIBusiness Operations
    WIZCOZ CORPORATION LTD690397273manufacture