Label: NATURALTH GOAT MILK MOISTURE- glycerin emulsion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated May 26, 2016

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  • ACTIVE INGREDIENT

    Active ingredient: Glycerin 6.00%

  • INACTIVE INGREDIENT

    Inactive Ingredient: Water,Goat Milk Extract,Hydrogenated Polydecene,Butylene Glycol,CetylEthylhexanoate,1,2-Hexanediol,Polysorbate60, ButyrospermumParkii(Shea)Butter, GlycerylStearate,Panthenol,Cetearyl Alcohol,Polyglyceryl-3Methylglucose Distearate,BiosaccharideGum-1,Phenoxyethanol,SorbitanStearate, Dimethicone,PalmiticAcid,Carbomer, PEG-100 Stearate, Stearic Acid, Tromethamine, Polyacrylate-13,Polyisobutene, Ethylhexylglycerin,XanthanGum, Fragrance, Disodium EDTA, Polysorbate 20,Pantolactone,SorbitanIsostearate, Lecithin, Alcohol, Polysorbate 80, Sodium AscorbylPhosphate,Ceramide3, Anthocyanins,CitricAcid,Hydrolyzed Hyaluronic Acid

  • PURPOSE

    Purpose: Skin Protectant

  • WARNINGS

    Warnings: For external use only. When using this product do not get into eyes. Stop use and ask a doctor if rash occurs. Do not use on - deep puncture wounds - animal bites - serious burns Keep out of reach of children.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • Use

    Use: Moisturizing seaweed lotion that supplies moisture to rough and dry skin

  • Directions

    Directions: - clean the skin thoroughly before using - apply in daily skin care routine

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    NATURALTH GOAT MILK MOISTURE 
    glycerin emulsion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59078-280
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Glycerin (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) Glycerin9 g  in 150 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Butylene Glycol (UNII: 3XUS85K0RA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59078-280-021 in 1 CARTON05/01/2016
    1NDC:59078-280-01150 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/01/2016
    Labeler - TONYMOLY CO.,LTD (688216798)
    Registrant - TONYMOLY CO.,LTD (688216798)
    Establishment
    NameAddressID/FEIBusiness Operations
    TONYMOLY CO.,LTD688216798manufacture(59078-280)
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