Label: ETHYL ALCOHOL solution

  • NDC Code(s): 54622-015-01
  • Packager: Georgia Pacific Consumer Products
  • 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 June 23, 2022

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  • Active ingredient

    Ethyl Alcohol 67% v/v

  • Purpose

    Antiseptic

  • Uses

    To decrease bacteria on skin that could cause disease

    Recommended for repeated use

  • Warnings

    FLAMMABLE, keep away from fire or flame

    For external use only

  • When using this product

     do not use in or near eyes.

  • Stop use and ask a doctor if

    irritation or redness develops.  If condition persists for more than 72 hours consult a doctor.

  • Keep out of reach of children.

    If swallowed, seek immediate medical attention or call a poison control center.

  • Directions

    Wet hands thoroughly with product and allow to dry without wiping.

  • Inactive ingredients

    water, isopropyl alcohol, Aloe barbadensis leaf juice, tocopheryl acetate, isopropyl myristate, glycerin, carbomer, diisopropylamine  

  • SPL UNCLASSIFIED SECTION

    enMotion Gel Hand Sanitizer with Moisturizers Fragrance Free

    SKU 42337

    Manufactured for Georgia-Pacific Consumer Products LP. Atlanta, GA 30303

    Quesitons? Call 1-866-HELLOGP (435-5647) or visit us online at www.gppro.com

    (c) 2017 Georgia Pacific Consumer Products LP. All rights reserved.

    alcohol permit SDS-MO-15036, DSP-MO-28, DSP-MO-34

    42336-7-V1PRDRevA L0016895BA

  • principal display panel

    Gel Hand Sanitizer with Moisturizers

    1000 mL (33.8 FL OZ)

    image description

  • INGREDIENTS AND APPEARANCE
    ETHYL ALCOHOL 
    ethyl alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54622-015
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.67 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CARBOMER 1342 (UNII: 809Y72KV36)  
    DIISOPROPYLAMINE (UNII: BR9JLI40NO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54622-015-011000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product07/03/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A07/03/2017
    Labeler - Georgia Pacific Consumer Products (806142217)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC790752542manufacture(54622-015)
    Establishment
    NameAddressID/FEIBusiness Operations
    Vi-Jon, LLC088520668manufacture(54622-015)
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