Label: INSTANT HAND SANITIZER KICKPRINTS- ethyl alcohol gel

  • 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 June 18, 2013

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

View All Sections
  • ACTIVE INGREDIENT

    Active Ingredient
    Ethyl Alcohol 62%
  • PURPOSE

    Purpose
    Antiseptic
  • INDICATIONS & USAGE

    Kills 99.99% of Germs With Moisturizers & Vitamin E
    Uses: Hand sanitizer to help decrease bacteria on the skin when water, soap & towel are not available. Recommended for repeated use.

  • WARNINGS

    Warnings: For external use only. Flammable. Keep away from fire or flame. 
    Do not apply around eyes. Do not use in ears or mouth.
    When using this product, avoid contact with eyes. In case of contact, flush eyes with water.
  • STOP USE

    Stop use and consult a doctor if redness or irritation develops and persists for more than 72 hours.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. 
    Use only under adult supervision.
  • DOSAGE & ADMINISTRATION

    Directions: Pump as needed into palms and thoroughly spread on both hands.                                                                                                                                                                         
    Rub into skin until dry. 
    Other information: Do not store in temperature above 118 F.  
  • PRINCIPAL DISPLAY PANEL

    image of bottle label
  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS:
    Water, Glycerin, Propylene Glycol, Carbomer
  • INGREDIENTS AND APPEARANCE
    INSTANT HAND SANITIZER KICKPRINTS  
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58948-1001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58948-1001-260 mL in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E06/18/2013
    Labeler - Empire Stationery Distributors Inc. (115360534)
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!