Label: FREE HAND SANITIZER- alcohol gel

  • NDC Code(s): 78304-005-01
  • Packager: BLAKEMORE SALES CORPORATION
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 24, 2024

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

View All Sections
  • Drug Facts

  • Active ingredient

    Ethyl Alcohol 70% v/v

    Purpose

    Antiseptic

  • Uses

    • helps reduce bacteria that potentially can cause disease
    • helps prevent cross contamination by hand contact
    • recommended for repeated use
  • Warnings

    For external use only.

    Flammable. Keep away from heat or flame.

    Do not use

    • in children less than 2 months of age or on open skin wounds

    When using this product

    • keep out of eyes and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

    Stop use and ask a doctor

    if irritation or redness develops.

    Keep out of reach of children.

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

  • Directions

    • Place enough product on hands to cover all surfaces.
    • Rub hands together until dry.
    • Supervise children under 6 years of age when using this product to avoid swallowing.
  • Other information

    • avoid freezing and excessive heat above 40°C(104°F)
    • may disolor certain fabrics
  • Inactive ingredients

    Water, Glycerin, Aloe Barbadensis Extract, Aminomethyl Propanol, Propylene Glycol, Carbomer, Fragrance, Tocopherol.

  • Package Labeling

    Label

  • INGREDIENTS AND APPEARANCE
    FREE HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78304-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78304-005-01500 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package05/22/202001/31/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)05/22/202001/31/2026
    Labeler - BLAKEMORE SALES CORPORATION (164380578)
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!