Label: GLYCOLIC ACID FACIAL WET COMPRESS WITH FRUIT ACID liquid

  • NDC Code(s): 84753-026-01
  • Packager: Guangdong Bisutang Biotechnology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 13, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • ACTIVE INGREDIENT

    SACCHARUM OFFICINARUM (SUGAR CANE) EXTRACT

  • PURPOSE

    After cleansing andtoning, take an appropriate amount ofthis product and apply it evenly on theface, massage until absorbed

  • Ask Doctor

    If you have a history of skin allergies or have sensitive skin, it is advisable to consult a doctor before using this product.

  • DOSAGE & ADMINISTRATION

    Apply once daily to clean face and neck, avoiding the eye area

  • WHEN USING

    Avoid contact with eyes and broken skin. If redness, swelling, or irritation occurs, discontinue use immediately and seek medical advice.

  • WARNINGS

    Risk InformationFor external use only
    Mention de risquesPour usage externe seulement
    Do not use on damaged or broken skin.
    Ne pas utiliser sur la peau endommagée ou avec des lésions
    If rash occurs, discontinue use and consult a health care practitioner.
    En présence d'une éruption cutanée, cesser l'utilisation et consulter un praticien de soins de santé
    When using this product keep out of eyes. Rinse with water to remove.
    Eviter tout contact avec les yeux. Rincer a l'eau le cas échéant
    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
    Tenir hors de portée des enfants
    En cas d'ingestion, consulter un médecin ou appeler un centre antipoison immédiatement.

  • INDICATIONS & USAGE

    Temporarily protects and helps relieve dry or cracked skin
    Beneficlal for face, hands, body, and legs

  • 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.
    Tenir hors de portée des enfants
    En cas d'ingestion, consulter un médecin ou appeler un centre antipoison immédiatement.

  • INACTIVE INGREDIENT

    GLYCERIN

    SODIUM HYDROXIDE
    SODIUM CARBONATE
    AQUA
    PROPYLENE GLYCOL
    DIAZOLIDINYL UREA
    IODOPROPYNYL BUTYLCARBAMATE
    HAMAMELIS VIRGINIANA (WITCH HAZEL) WATER
    PHENOXYETHANOL
    HYDROXYETHYLCELLULOSE
    PEG-50 HYDROGENATED CASTOR OIL
    MENTHOL
    NONOXYNOL-12
    PROPYLENE GLYCOL
    MENTHYL LACTATE
    PEG-35 CASTOR OIL
    METHYLPARABEN
    PANTHENOL
    PROPANEDIOL
    CAPRYLIC/CAPRIC TRIGLYCERIDE
    POLYGLYCERYL-10 MYRISTATE
    POLYSORBATE 80
    ISONONYL ISONONANOATE
    RETINYL PALMITATE
    TOCOPHERYL ACETATE
    HYDROGENATED LECITHIN
    BHT
    AQUA
    BUTYLENE GLYCOL
    CAMELLIA SINENSIS LEAF EXTRACT
    PHENOXYETHANOL
    AQUA
    BUTYLENE GLYCOL
    CHRYSANTHELLUM INDICUM EXTRACT
    PHENOXYETHANOL

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    GLYCOLIC ACID FACIAL WET COMPRESS WITH FRUIT ACID 
    glycolic acid facial wet compress with fruit acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84753-026
    Route of AdministrationCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SACCHARUM OFFICINARUM WHOLE (UNII: 3Z20C92XNB) (SACCHARUM OFFICINARUM WHOLE - UNII:3Z20C92XNB) SACCHARUM OFFICINARUM WHOLE8.4 g  in 240 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    PEG-50 HYDROGENATED CASTOR OIL (UNII: R07D3A9614)  
    HYDROXYETHYLCELLULOSE (UNII: T4V6TWG28D)  
    DEXPANTHENOL (UNII: 1O6C93RI7Z)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84753-026-01240 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/10/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)11/10/2024
    Labeler - Guangdong Bisutang Biotechnology Co., Ltd. (447075429)
    Registrant - Guangdong Bisutang Biotechnology Co., Ltd. (447075429)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangdong Bisutang Biotechnology Co., Ltd.447075429manufacture(84753-026)