Label: HARMON FACE VALUES WARM VANILLA SUGAR SCENT HAND SANITIZER- 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 November 17, 2022

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

View All Sections
  • Active Ingredient

    Ethyl Alcohol 62%

    Purpose

    Antibacterial

  • 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 or ask for a doctor if redness or irritation develops and persists for more than 72 hours.

  • Keep out of reach of children.

    Children must be supervised in use of this product.

  • Directions

    Squeeze as needed into your palms and thoroughly spread on both hands. Rub into skin until dry

  • Other Information

    Do not store in temperatures over 118 degress F.

  • Inactive Ingredients

    Alcohol, Water, Aloe barbadensis leaf juice, glycerin, propylene glycol, carbomer, triethanolamine, fragrance, FDandC Blue 1, FDandC yellow 5, FDandC red 4.

  • Dist. by Harmon Stores, Inc.,

    650 Liberty Ave.

    Union, NJ 07083 Made in China

  • Product Labeling

    label

  • INGREDIENTS AND APPEARANCE
    HARMON FACE VALUES WARM VANILLA SUGAR SCENT HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63940-613
    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)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63940-613-0258 mL in 1 BOTTLE; Type 0: Not a Combination Product08/23/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A08/23/2013
    Labeler - Harmon Stores Inc. (804085293)
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!