Label: ENMOTION FOAM SANITIZER WITH MOISTURIZERS FRAGRANCE FREE- ethyl alcohol solution

  • 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 March 23, 2021

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  • Active Ingredient

    Ethyl Alcohol 70% 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

    When using this product do not use in or near eyes.

  • STOP USE

    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*, PEG-12 Dimethicone, Glycerin, Hydrolyzed Jojoba Esters, Caprylic/Capric Triglyceride, Panthenol, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Blue 1, Yellow 5.

    *may contain this ingredient

  • Rear Label Text

    enMotion®

    Foam Hand Sanitizer with Moisturizers

    E3-Rated • Fragrance Free • SKU 42334

    Manufactured for

    Georgia-Pacific Consumer Products. Atlanta, GA 30303-2529

    Questions? Call 1-866-HELLOGP (435-5647)

    or visit us online at www.gppro.com

    ©2020 GP PRO. All rights reserved.

    alcohol permit SDS-NJ-20007

    5000011192/000/00

  • PRINCIPAL DISPLAY PANEL

    Foam Hand Sanitizer with Moisturizers

    1000 mL (33.8 FL OZ)

    NDC - 54622-423-01

    FrontRear

  • INGREDIENTS AND APPEARANCE
    ENMOTION FOAM SANITIZER WITH MOISTURIZERS FRAGRANCE FREE 
    ethyl alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54622-423
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    PEG-12 DIMETHICONE (UNII: ZEL54N6W95)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54622-423-011000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product06/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/01/2021
    Labeler - Georgia Pacific Consumer Products (806142217)
    Registrant - Accupac, LLC (071609663)
    Establishment
    NameAddressID/FEIBusiness Operations
    Accupac, LLC061595175manufacture(54622-423)
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