Label: ANTIBACTERIAL HAND SANITIZER- alcohol gel

  • NDC Code(s): 70204-100-30
  • Packager: Hit Promotional Products
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 21, 2023

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

View All Sections
  • Drug Facts

  • Active Ingredients

    Ethyl Alcohol 62%

    Purpose

    Antiseptic

  • Uses:

    Hand sanitizer to help decrease bacteria on the skin.  When water, soap & towel are not available.  Recommended for repeated use.

  • Warnings:

    For external use only.  Flammable.  Keep away from fire or flame.  Do not apply around eyes.

    Do not use

    in ears & mouth.

    When using this product,

    avoid contact with eyes.  In case of contact flush eyes with water.

    Stop use and ask a doctor

    if redness or irritation develop and persist for more than 72 hours.

    Keep out of reach of children.

    Children must be supervised in use of this product.

  • Directions:

    Squirt as needed into your palms and thoroughly spread on both hands.  Rub into skin until dry

  • Other Information:

    Store at 20 ​o​C (68 ​o​ to 77 ​o​F).  May discolor fabrics

  • Inactive Ingredients:

    water, triethanolamine, glycerin, propylene glycol, tocopheryl acetate, carbomer, fragrance.

  • Package Labeling:

    DrugFacts

  • INGREDIENTS AND APPEARANCE
    ANTIBACTERIAL HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70204-100
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL620 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70204-100-3030 mL in 1 BOTTLE; Type 0: Not a Combination Product05/24/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)05/24/2016
    Labeler - Hit Promotional Products (081070202)
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!