Label: ANTIBACTERIAL HAND SANITIZER- triclosan liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated September 23, 2020

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

View All Sections
  • Drug Facts

  • Active ingredient

    Triclosan 0.25%

    Purpose

    Antiseptic

    USE

    For handwashing to decrease bacteria on the skin.

  • Warnings

    For external use only.

    When using this product

    Avoid direct contact with eyes. In case of contact with eyes, rinse immediately with plenty of water

    Stop use and ask a doctor

    • If irritation persists, get medical attention.

    Keep out of reach of children.

    If swallowed, seek medical advice immediately and show this container or label.

  • Directions

    • Wet your hands with running water, get some hand sanitizer on hands, rub your hands away from each other, and rub the back of your hands, fingers, palms, and nail seams repeatedly in a circular motion.
    • After about 2 minutes, rinse the foam with hands under running water.
    • Wipe hands with a dry cloth

    Other Information:

    Store below 110℉（43℃）

  • Inactive ingredients

    Water、Sodium Laureth Sulfate、Sodium Taurine Cocoyl Methyltaurate、Cocamidiopropyl Betaine、Glycerin、Cocamide MEA、Aloe Vera Extract、Citric Acid、Tocopherol、Disodium EDTA

  • package

    label image

  • INGREDIENTS AND APPEARANCE
    ANTIBACTERIAL HAND SANITIZER 
    triclosan liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80155-102
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN2.5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80155-102-01250 mL in 1 BOTTLE; Type 0: Not a Combination Product09/23/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E09/23/2020
    Labeler - HangZhou Vivian Household Products Co.,Ltd (540103625)
    Establishment
    NameAddressID/FEIBusiness Operations
    HangZhou Vivian Household Products Co.,Ltd540103625manufacture(80155-102)
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!