Label: GOLDKIWI- dimethicone 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 July 27, 2011

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Active ingredient: DIMETHICONE 6.7%

  • INACTIVE INGREDIENT

    Inactive ingredients:

    WATER, ACTINIDIA CHINENSIS (KIWI) FRUIT EXTRACT, TRISILOXANE, PROPYLENE GLYCOL, BETA-GLUCAN, GLYCERIN, NIACINAMIDE,  BETAINE, BUTYLENE GLYCOL, DIISOSTEARYL MALATE, HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, MACADAMIA TERNIFOLIA SEED OIL, PEG-40 STEARATE, POLYGLYCERYL-3 METHYLGLUCOSE DISTEARATE, CETYL ETHYLHEXANOATE, CYCLOPENTASILOXANE, LACTOBACILLUS FERMENT LYSATE FILTRATE, TRIMETHYLSILOXYSILICATE, C14-22 ALCOHOLS, C12-14 PARETH-12, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, MAACKIA FAURIEI STEM EXTRACT, C12-20 ALKYL GLUCOSIDE, CITRULLUS VULGARIS (WATERMELON) FRUIT EXTRACT, PRUNUS MUME FRUIT EXTRACT, NYMPHAEA ALBA FLOWER EXTRACT, SODIUM PALMITOYL PROLINE, DISODIUM EDTA, SODIUM HYALURONATE, XANTHAN GUM, AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER, DISODIUM COCOAMPHODIACETATE, PANTHENOL, SACCHAROMYCES CEREVISIAE EXTRACT, TRITICUM VULGARE (WHEAT) GERM EXTRACT, METHYLPARABEN, PROPYLPARABEN, PHENOXYETHANOL, FRAGRANCE

  • PURPOSE

    Purpose:

    This combination of cosmetics is used for your basic skin care and gives a benefit for Brightening care.

  • WARNINGS

    Warnings:

    For external use only. Avoid contact with eyes. Discontinue use if signs of irritation appear.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children:

    Keep out of reach of children.

  • INDICATIONS & USAGE

    Indication and usage:

    Following emulsion, pour some on the palm of your hand and apply to skin gently. Press down lightly until absorbed.

  • DOSAGE & ADMINISTRATION

    Dosage and administration:

    Take appropriate amount according to your skin condition and apply every morning and night.

  • PRINCIPAL DISPLAY PANEL

    Image of bottle

  • INGREDIENTS AND APPEARANCE
    GOLDKIWI 
    dimethicone cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76214-002
    Route of AdministrationCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE3.69 g  in 55 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ACTINIDIA CHINENSIS SEED (UNII: 53V4NSR15J)  
    TRISILOXANE (UNII: 9G1ZW13R0G)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    BETAINE (UNII: 3SCV180C9W)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    MACADAMIA OIL (UNII: 515610SU8C)  
    PEG-40 STEARATE (UNII: ECU18C66Q7)  
    CETYL ETHYLHEXANOATE (UNII: 134647WMX4)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    C14-22 ALCOHOLS (UNII: B1K89384RJ)  
    MAACKIA FLORIBUNDA STEM (UNII: 84UXW52K8Y)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA)  
    PRUNUS MUME FRUIT (UNII: 639190I8CU)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    NYMPHAEA ALBA FLOWER (UNII: 40KQ7Q535O)  
    SODIUM PALMITOYL PROLINE (UNII: 64L053FRFO)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)  
    WHEAT GERM (UNII: YR3G369F5A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76214-002-0155 g in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34703/01/2011
    Labeler - SKINFOOD CO., LTD. (690324173)
    Registrant - SKINFOOD CO., LTD. (690324173)
    Establishment
    NameAddressID/FEIBusiness Operations
    SKINFOOD CO., LTD.690324173manufacture