Label: DIAPIA ADL TURMERIC PEARL FOAMING CLEANSER- glycerin liquid

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

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated October 29, 2020

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  • ACTIVE INGREDIENT

    glycerin

  • INACTIVE INGREDIENT

    Myristic Acid
    Palmitic Acid
    Potassium Hydroxide
    Stearic Acid
    Propylene Glycol
    Lauric Acid
    Beeswax
    Cocamidopropyl Betaine
    Glycol Distearate
    Sorbitan Olivate
    Sodium Hyaluronate
    Phenoxyethanol
    PEG-100 Stearate
    Glyceryl Stearate
    Fragrance
    Polyglutamic Acid
    Pearl Extract
    Curcuma Longa (Turmeric) Root
    Powder
    Disodium EDTA
    Propolis Extract

  • PURPOSE

    cleanse the skin

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    Put the appropriate amount onto wet hands and create dense foam. Gently massage your face, and then wash with lukewarm water.

  • WARNINGS

    1.Keep out of reach of children.

    2.Store in a cool, dry place and avoid direct sunlight.

    3.If abnormal symptoms occur after use, stop use and consult with a skin specialist.

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    DIAPIA ADL TURMERIC PEARL FOAMING CLEANSER 
    glycerin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71857-0014
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71857-0014-1120 mL in 1 TUBE; Type 0: Not a Combination Product10/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/30/2020
    Labeler - BSG H & B Co., Ltd. (694252895)
    Registrant - BSG H & B Co., Ltd. (694252895)
    Establishment
    NameAddressID/FEIBusiness Operations
    BSG H & B Co., Ltd.694252895manufacture(71857-0014) , label(71857-0014)