Label: JISBERRY ANTIBACTERIAL HANDLOTION- triclosan lotion

  • 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 April 26, 2020

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

  • DOSAGE & ADMINISTRATION

    Keep it away from Iight and store tina cool and dry place.

  • INACTIVE INGREDIENT

    Water

    Sodium Laureth Sulfate

    Cocamide DEA

    Citric Acid

    Sodium Chloride

    Pigments

  • INDICATIONS & USAGE

    1.Hand washing before surgery: Wet hands with flowing water first, then apply a proper amount of liquid into hands, wash hands, forearms and lower 1/3 of upper arm according to the requirements of hand hygiene standards, rub thoroughly for 2 minutes and rinse with flowing water.
    2.Sanitary hand washing: Wet hands with flowing water first, then apply a proper amount of liquid into hands, rub evenly and thoroughly for 2 minutes according to the requirements of hand hygiene standards, and rinse with flowing water.

  • ACTIVE INGREDIENT

    Triclosan

  • KEEP OUT OF REACH OF CHILDREN

    keep out of children

  • PURPOSE

    Disinfection
    Sterilization

  • WARNINGS

    1.This product is for external use and must not be taken orally. Keep it out ofchildren's reach.
    2.Immediately rinse with clean water if in contact with eyes.
    3.Keep it away from light and store it in a cool and dry place.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    JISBERRY ANTIBACTERIAL HANDLOTION 
    triclosan lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52738-005
    Route of AdministrationEXTRACORPOREAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN2 g  in 500 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    CHLOROPHYLL (UNII: 00WNZ48OR9)  
    COCO DIETHANOLAMIDE (UNII: 92005F972D)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52738-005-01500 mL in 1 BOTTLE; Type 0: Not a Combination Product04/12/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other04/12/2020
    Labeler - Hangzhou Xizi Sanitary Disinfection Medical Equipment Co., Ltd (527389022)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hangzhou Xizi Sanitary Disinfection Medical Equipment Co., Ltd527389022manufacture(52738-005)