Label: NITOUCH ALCOHOL HAND SANITIZER- ethyl alcohol spray

  • Category: HUMAN OTC DRUG LABEL

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 September 9, 2020

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • Drug Facts

  • ACTIVE INGREDIENT

    Active ingredients   Ethyl Alcohol 80% (v/v)

  • PURPOSE

    Purpose    Antiseptic

  • Uses

    • Hand Sanitizer

    • For use when soap and water are not available.

  • Warnings

    • Flammable. Keep away from fire or flame.

    • 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. Do not inhale

       or ingest.

    • Do not use in children less than 2 months of age.

    • Stop use and ask a doctor if irritation or a rash develops.

    • Keep out of reach of children. If swallowed, get medical help immediately and contact a Poison Control Center immediately.

  • Directions

    • Apply enough product to cover hand thoroughly.

    • Rub hands together, until hands feel dry. Do not rinse.

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

  • Other information

    • Store below 105°F (40°C). May discolor some fabrics

    • Avoid freezing and excessive heat above 105°F (40°C).

  • Inactive ingredients

    Aqua (Water), Glycerine, Fragrance, Hydrogen Peroxide, CI 42090

  • SPL UNCLASSIFIED SECTION

    For external use only

    Distributed by:

    Kasa Trading, LLC

    4500 E. Speedway Blvd

    Tucson, AZ 85712

    www.kasatrading.com

    Made in India

  • Packaging

    untitled

  • INGREDIENTS AND APPEARANCE
    NITOUCH ALCOHOL HAND SANITIZER 
    ethyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80437-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL80 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80437-002-01250 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product09/08/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A09/08/2020
    Labeler - Kasa Trading, Llc (080477332)
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

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!