Label: C19 ANTIMICROBIAL HAND SANITIZER- alcohol gel

  • NDC Code(s): 73369-0009-1, 73369-0009-2, 73369-0009-3, 73369-0009-4
  • Packager: Kabana Skin Care LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 23, 2024

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

View All Sections
  • ACTIVE INGREDIENT

    Ethyl Alcohol 70% v/v.

    PURPOSE

    Antimicrobial

  • USE

    Hand Sanitizer to help reduce pathogens on the skin.

  • WARNINGS

    FLAMMABLE. KEEP AWAY FROM FIRE OR FLAME.

    THIS PRODUCT IS INTENDED FOR EXTERNAL USE ONLY.

    DISCONTINUE USE IF irritation or redness develops.
    If condidtion persists for more than 72 hours, consult a doctor.

  • Do not use

    DISCONTINUE USE IF irritation or redness develops.

    If condition persists for more than 72 hours, consult a doctor.

  • WHEN USING

    WHEN USING THIS PRODUCT, Do not use in or near the eyes.

    In case of contact, rinse eyes thoroughly with water.

  • STOP USE

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • DIRECTIONS

    • Place enough product in your palm to throroughly cover your hands.
    • Rub hands together briskly until dry.
    • Children under 6 years of age should be supervised when using this product.
  • OTHER INFORMATION

    • Store below 110F (44C)
    • May discolor certain fabrics or surfaces
  • INACTIVE INGREDIENTS

    Water (aqua), Hydroxyethylcellulose

  • Package Label

    C19 Antimicrobial Hand Sanitizer

  • INGREDIENTS AND APPEARANCE
    C19 ANTIMICROBIAL HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73369-0009
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL64.7 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) 1.2 g  in 100 g
    WATER (UNII: 059QF0KO0R) 34.1 g  in 100 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73369-0009-178 g in 1 TUBE; Type 0: Not a Combination Product04/03/2020
    2NDC:73369-0009-2206 g in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product04/03/2020
    3NDC:73369-0009-43359 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/03/2020
    4NDC:73369-0009-3822 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product04/03/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/03/2020
    Labeler - Kabana Skin Care LLC (080237112)
    Registrant - Kabana Skin Care LLC (080237112)
    Establishment
    NameAddressID/FEIBusiness Operations
    Kabana Skin Care LLC080237112manufacture(73369-0009)
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!