Label: FA HAND SANITIZER GEL 70% (ETHANOL)- hand sanitizer gel

  • NDC Code(s): 74932-100-01
  • Packager: HLB CO.,LTD_Healthcare
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 7, 2024

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

View All Sections
  • Active Ingredient

    Ethyl Alcohol 70%

  • Purpose

    Antiseptic

  • Use

    Hand Sanitizer to help reduce bacteria on the skin.

    Recommended for repeated use.

  • Warnings

    For external use only - hands

    Flammable, Keep awa from fire or flame

  • When useing this product

    -do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

    -avoid contact with broken skin.

    -do not inhale or ingest.

  • Stop use and ask a doctor if

    irritation or rash appears and lasts.

  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poision Control Center right away.

  • Directions

    Place enough product in your palm to thoroughly cover your hands.

    Rub hands together briskly until dry.

    Children under 6 years of age should be supervised when using this product.

    Not recommended for infants.

  • Other information

    Store below 86 oF (Between 1 oC-30 oC).

    May discolor certain fabrics or surfaces.

  • Inactive Ingredients

    Carbormer, Fragrance, Glycerin, Triethanolamine, Water.

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    FA HAND SANITIZER GEL 70% (ETHANOL) 
    hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74932-100
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    WATER (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74932-100-011 in 1 BOX04/10/2020
    157 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00304/10/2020
    Labeler - HLB CO.,LTD_Healthcare (987587913)
    Registrant - HLB CO.,LTD_Healthcare (987587913)
    Establishment
    NameAddressID/FEIBusiness Operations
    HLB CO.,LTD_Healthcare987587913manufacture(74932-100)
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!