Label: LIQUID HAND CLEANSE- triclosan gel

  • NDC Code(s): 57337-016-01
  • Packager: Rejoice International, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 28, 2024

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  • ACTIVE INGREDIENT

    Active Ingredient                 Purpose

    Triclosan 0.2%......................Antiseptic

  • PURPOSE

    Health Care Instant Hand Sanitizer - Ice Clear - Extra Enriched with Vitamin E Bead & Aloe

    Kills 99.9% of Germs without water or towels!

  • 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.

  • INDICATIONS & USAGE

    USE: 

    • handwashing to decrease bacteria on the skin
  • WARNINGS

    Warnings:

    for external use only.

    Flammable. Keep away from heat and flame.

    Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.

    Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.

  • DOSAGE & ADMINISTRATION

    Directions:

    • wet hands thoroughly with product
    • briskly rub hands together until dry
    • supervise children in the use of this product
  • INACTIVE INGREDIENT

    Inactive ingredients:

    aloe vera leaf juice, carbomer, glycerin, propylene glycol, tocopheryl acetate (vitamin E), triethanolamine, water.

  • PRINCIPAL DISPLAY PANEL

    bottle label

  • INGREDIENTS AND APPEARANCE
    LIQUID HAND CLEANSE 
    triclosan gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57337-016
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN10 mg  in 500 mg
    Inactive Ingredients
    Ingredient NameStrength
    CETETH-7 (UNII: 4ST6952Q67)  
    ETHYL SULFATE (UNII: P3LK0HF3B7)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    DIETHANOLAMINE (UNII: AZE05TDV2V)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    OCTHILINONE (UNII: 4LFS24GD0V)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57337-016-01500 mg in 1 BOTTLE; Type 0: Not a Combination Product07/05/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00307/05/2013
    Labeler - Rejoice International, Inc. (078741245)
    Establishment
    NameAddressID/FEIBusiness Operations
    China Ningbo Shangge Cosmetic Technology Corp.529287434manufacture(57337-016)
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