Label: ALCOHOL liquid

  • NDC Code(s): 41163-975-16, 41163-975-34, 41163-975-45
  • Packager: United Natural Foods, Inc. dba UNFI
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 17, 2026

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

View All Sections
  • Active ingredient

    Ethyl Alcohol 62%

  • Purpose

    Antiseptic

  • Uses

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

    For external use only: hands

    Flammable, keep away from fire or flame.

  • When using this product

    • keep out of eyes.  In case of contact with eyes, flush thoroughly with water.
    • avoid contact with broken skin
    • do not inhale or ingest
  • Stop use and ask a doctor if

    • irritation and redness develop
    • condition persists for more than 72 hours
  • Keep out of reach of children.

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

  • Directions

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

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

    water, carbomer and/or acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, glycerin, isopropyl myristate, tocopheryl acetate

  • ADVERSE REACTION

    Like it or let us make it right.

    That's our quality promise.

    855-423-2630

    DISTRIBUTED BY UNFI

    PROVIDENCE, RI 02908 USA

    DSP-TN-21091

    DSP-MO-20087

  • Principal display panel

    EQUALINE ®

    MOISTURIZING

    Hand Sanitizer

    with Vitamin E

    32 FL OZ (1 QT) 946 mL

    image descriptionimage description

  • INGREDIENTS AND APPEARANCE
    ALCOHOL 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-975
    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)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41163-975-1659 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/02/2023
    2NDC:41163-975-34236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/02/2023
    3NDC:41163-975-45946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/02/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)02/02/2023
    Labeler - United Natural Foods, Inc. dba UNFI (943556183)
    Registrant - Nice-Pak Products, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nice-Pak Products, LLC119091514manufacture(41163-975)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nice-Pak Products, LLC119091520manufacture(41163-975)
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!