Label: FOASU JIN POWDERWASH- allantoin, panthenol powder

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

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Drug Label Information

Updated February 27, 2022

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  • Active ingredient

    allantoin, panthenol

  • Purpose

    skin protectant

  • Use

    apply proper amount to the skin, or the enclosed bubble pad, wet it with water, make enough bubbles, massage gently all over the face, and rinse thoroughly with warm water

  • Warnings

    For external use only

    1) Please consult your doctor if you experience side effects such as swelling, itching, or reddening on the area where you applied this product

    2) Do not apply on wounds or cuts. 3) Do not store where children may reach, and avoid keeping it exposed to direct sunlight.

  • Directions

    for external use only

  • Inactive ingredients

    ZEA MAYS (CORN) STARCH
    SODIUM LAUROYL GLUTAMATE
    SODIUM COCOYL GLUTAMATE
    MANNITOL
    BETAINE
    PAPAIN
    CELLULOSE GUM
    ARTEMISIA VULGARIS EXTRACT
    ETHYLHEXYLGLYCERIN
    CENTELLA ASIATICA EXTRACT
    CENTELLA ASIATICA EXTRACT
    BROMELAIN
    DISODIUM EDTA
    ANGELICA GIGAS ROOT EXTRACT
    BLETILLA STRIATA ROOT EXTRACT
    PORIA COCOS EXTRACT
    ANGELICA TENUISSIMA ROOT EXTRACT
    POLYGONATUM OFFICINALE RHIZOME/ROOT EXTRACT
    CNIDIUM OFFICINALE ROOT EXTRACT
    ECTOIN
    BUTYLENE GLYCOL
    WATER
    1,2-HEXANEDIOL
    PEARL POWDER

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    FOASU JIN POWDERWASH 
    allantoin, panthenol powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:77964-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN0.1 g  in 100 g
    PANTHENOL (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z) PANTHENOL0.01 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:77964-005-0170 g in 1 CONTAINER; Type 0: Not a Combination Product02/27/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other02/27/2022
    Labeler - HANSCOS Co.,Ltd. (688494423)
    Registrant - HANSCOS Co.,Ltd. (688494423)
    Establishment
    NameAddressID/FEIBusiness Operations
    HANSCOS Co.,Ltd.688494423manufacture(77964-005)
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