Label: CVS HAND SANITIZER- 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 December 8, 2020

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

View All Sections
  • Active Ingredients

    Alcohol 70% v/v..................................................................Antiseptic

  • Purpose

    Antiseptic

  • Uses

    hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available

  • Warnings

    For external use only

    Do not use

    in children less than 2 months of age.

    on open skin wounds

    When using this product

    keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

    Stop use and ask a doctor

    Irritation or rash occurs. These may be signs of a serious condition

    Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center right away

  • Directions

    Place enough product on hands to cover all surfaces. Rub hands together until dry.
    Supervise children under 6 years of age when using this product to avoid swallowing

  • Other Information

    Store between 15–30 °C (59–86 °F)
    Avoid freezing and excessive heat above 40 °C (104 °F)
    Close cap after use
    May discolor certain fabrics or surfaces

  • Inactive Ingredients

    acrylates/C10–30 alkyl acrylate crosspolymer, aminomethyl propanol, glycerin, isopropyl myristate,propylene glycol, purified water, SD alcohol 40-B, tocopheryl acetate

  • PRINCIPAL DISPLAY PANEL

    LabelCVS Health

    Moisturizing Hand Sanitizer Gel

    With Vitamin E

    70% ethyl alcohol

    Paraban & phthalate free

  • INGREDIENTS AND APPEARANCE
    CVS HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-760
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69842-760-0259 mL in 1 BOTTLE; Type 0: Not a Combination Product12/08/2020
    2NDC:69842-760-08236.5 mL in 1 BOTTLE; Type 0: Not a Combination Product12/08/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A12/08/2020
    Labeler - CVS (062312574)
    Registrant - WEEKS & LEO COMPANY, INC. (005290028)
    Establishment
    NameAddressID/FEIBusiness Operations
    WEEKS & LEO COMPANY, INC.005290028manufacture(69842-760)
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!