Label: WALGREENS- 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 November 8, 2022

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

View All Sections
  • ACTIVE INGREDIENT

    Ethyl Alcohol 70%

  • PURPOSE

    Antiseptic

  • INDICATIONS & USAGE

    • to decrease bacteria on the skin that could cause disease
    • recommended for repeated use
  • WARNINGS

    For external use only-hands

    Flammable. Keep away from heat and flame.

    -keep out of eyes. In case of contact with eyes, flush thoroughly with water
    -avoid contact with broken skin
    -do not inhale or ingest

    -irritation or redness develops
    -condition persists for more than 72 hours

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

  • DOSAGE & ADMINISTRATION

    • wet hands thoroughly with product and allow to dry without wiping
    • for children under 6, use only under adult supervision
    • not recommended for infants
  • STORAGE AND HANDLING

    • do not store above 105⁰ F
    • may discolor some fabrics
    • harmful to wood finishes and plastics
  • INACTIVE INGREDIENT

    Isopropyl alcohol, glycerin, isopropyl myristate, tocopheryl acetate, water, PEG 6 AMP-Acrylates/Vinyl Isodecanoate, fragrance, blue 1, violet 2

  • PRINCIPAL DISPLAY PANEL

    59 mL

  • INGREDIENTS AND APPEARANCE
    WALGREENS 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-5721
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL700 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    VAT VIOLET 2 (UNII: ZVX9A7UOON)  
    MPEG 6000 ACETYL LYSINE (UNII: 83L9KWH0UW)  
    FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-5721-0459 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/19/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A10/19/2022
    Labeler - walgreens (008965063)
    Registrant - Apollo Health and Beauty Care (201901209)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apollo Health and Beauty Care201901209manufacture(0363-5721)
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!