Label: HAND SANITIZER- hand sanitizer foam bac spray

  • 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 December 27, 2022

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

View All Sections
  • Supersource Hand Sanitizer

    Alcohol Free

    Net Contents:3.4 FL OZ. (100mL)

    NDC: 75056-009-34

    Item No: CLE225

    Atlanta Supersource, Inc.

    3655 Kennesaw 75 Parkway, Suite 100

    Kennesaw, GA 30144

  • Active Ingredient

    Benzalkonium Chloride 0.1%

  • Purpose

    Antimicrobial

  • Uses

    Hand Sanitizer to help reduce bacteria that can potentially cause disease. For use when soap and water are not available. Recommended for repeated use.

  • Warnings

    For external use only.

  • When using this product

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

  • Stop use and ask doctor

    if irritation or rash occurs.

  • 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.

  • Inactive Ingredients

    Water, Cetrimonium Chloride, Laurtrimonium Chloride, Dihydroxyethyl Cocamine Oxide, Glycereth-17 Cocoate, Citric Acid Monohydrate, Fragrance.

  • Questions or Comments?

    Call us at 833.423.0006

  • Signature Hand Sanitizer Alcohol Free

    Item LabelNET CONTENTS: 3.4 OZ (100mL)

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    hand sanitizer foam bac spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75056-009
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 99.8703 g  in 100 g
    DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5) 0.0099 g  in 100 g
    LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC) 0.0099 g  in 100 g
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP) 0.0099 g  in 100 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75056-009-34100 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E01/01/2021
    Labeler - Atlanta Supersource, Inc. (806786778)
    Establishment
    NameAddressID/FEIBusiness Operations
    Atlanta Supersource, Inc.806786778manufacture(75056-009)
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!