Label: PEPPERMINT HAND SANITIZER- ethyl alcohol liquid

  • 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 29, 2011

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

View All Sections
  • Active Ingredient

    Ethyl Alcohol 62%

  • Purpose

    Sanitizer

  • Uses

    To decrease bacteria on the skin that could cause disease.

    recommended for repeated use

  • Warnings

    For external use only-hands. Use only as directed. Excessive use or prolonged exposure may cause irritation to skin. Discontinue use if rash redness or itching occurs

    Flammable. keep away from heat and flame.

  • When using this product

    keep out of eyes. In case of contact with eyes immediately flush with water and call a doctor

    avoid contact with broken skin.

  • STOP USE

    Stop use and ask a doctor if irritation or redness develops.

  • Keep out of reach of children.

    In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

  • Directions

    put a thumb size amount in your palm and rub hands together briskly until dry. recommended for repeated use.

  • Other Information

    do not store in temperatures over 118F.

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

    may discolor certain fabrics.

  • Inactive Ingredients

    aloe barbadensis gel, blue 1, carbomer, deionized water, fragrance, glycerin, propylene glycol, triethanolamine, vitamin E, and Yellow 5

  • PRINCIPAL DISPLAY PANEL

    Peppermint
    Hand sanitizer

    net .95fl oz (28ml)

  • PRINCIPAL DISPLAY PANEL

    Vanilla Hand Sanitizer

  • INGREDIENTS AND APPEARANCE
    PEPPERMINT HAND SANITIZER 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75997-028
    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
    ALOE (UNII: V5VD430YW9)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75997-028-0128 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/28/2011
    Labeler - Papermates, Inc. dba Noteworthy (038734620)
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!