Label: ALCOHOL liquid

  • NDC Code(s): 41163-826-16, 41163-826-34
  • Packager: United Natural Foods, Inc. dba UNFI
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 8, 2024

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  • 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
    • aoid contact with broken skin
    • do not inhale of 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 105° F
    • may discolor some fabrics
    • harmful to wood finishes and plastics
  • Inactive ingredients

    water, carbomer, fragrance, glycerin, isopropyl myristate, Aloe barbadensis leaf juice, tocopheryl acetate, blue 1, yellow 5

  • Adverse reaction

    Like it or let us make it right.

    That's our quality promise.

    855-423-2630

    DISTRIBUTED BY UNFI

    PROVIDENCE, RI 02968 USA

  • Principal display panel

    EQUALINE

    MOISTURIZING

    Hand Sanitizer

    with Aloe and Vitamine E

    2 FL OZ (59 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    ALCOHOL 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-826
    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
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    ALOE (UNII: V5VD430YW9)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41163-826-34236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/13/2022
    2NDC:41163-826-1659 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/13/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/13/2022
    Labeler - United Natural Foods, Inc. dba UNFI (943556183)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091520manufacture(41163-826)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(41163-826)
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