Label: HAND CLEANSER (hand cleanser- amber 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 December 28, 2021

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

View All Sections
  • ACTIVE INGREDIENT

    LAURETH-10 6%

    Glycerin 3%

    Amber extract 10.2%

  • INACTIVE INGREDIENT

    Deionized water

    AMINO ACIDS, APRICOT KERNEL

    WHITE WAX

  • HOW TO USE

    Squeeze an appropriate amount of this product in your hands and scrub it, then rinse it with clean water.

  • DIRECTIONS

    This product is used to clean hands.

    Children should be supervised when using this product

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • PURPOSE

    clean

  • STORAGE AND HANDLING

    Keep in a cool and dry place

  • WARNINGS

    Do not take orally, for external use only.

    When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask doctor if irritation or rash appears and lasts.Keep out of reach of children.
    lf swallowed, get medical help or contact a Poison Control Center right away.

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    HAND CLEANSER 
    hand cleanser(amber) liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82371-008
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMBER (UNII: 70J9Z0J26P) (AMBER - UNII:70J9Z0J26P) AMBER10.2 g  in 100 mL
    LAURETH-10 (UNII: BD7AST04GA) (LAURETH-10 - UNII:BD7AST04GA) LAURETH-106 g  in 100 mL
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    WHITE WAX (UNII: 7G1J5DA97F)  
    AMINO ACIDS, APRICOT KERNEL (UNII: 29W70FJS26)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82371-008-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product12/29/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/29/2021
    Labeler - Zhejiang Dibao Biotechnology Co., Ltd. (603023294)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Dibao Biotechnology Co., Ltd.603023294manufacture(82371-008)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!