Label: ENMOTION FOAM HAND SANITIZER- ethyl alcohol liquid

  • NDC Code(s): 54622-120-01, 54622-120-02
  • Packager: Georgia-Pacific Consumer Products LP
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 15, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient

    Ethyl Alcohol 70% v/v

  • PURPOSE

    Purpose

    Antiseptic

  • INDICATIONS & USAGE

    Uses

    • To decrease bacteria on skin that could cause disease
    • Recommended for repeated use
  • WARNINGS

    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 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.

  • DOSAGE & ADMINISTRATION

    Directions

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

  • INACTIVE INGREDIENT

    Inactive ingredients Water, Isopropyl Alcohol, PEG-12 Dimethicone, Glycerin, Hydrolyzed Jojoba Esters, Caprylic/Capric Triglyceride, Panthenol, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, FD&C Blue #1, FD&C Yellow #5

  • SPL UNCLASSIFIED SECTION

    enMotion

    Foam Hand Sanitizer with Moisturizers

    E3-Rated Frgrance Free SKU 42334

    NSF

    NonfoodCompounds

    Program Listed E3

    Registration 152100

    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

    © 2018 GP PRO. All rights reserved.

    alcohol permit SDS-KY-15002

    42334-B2 PRDRevA

  • PRINCIPAL DISPLAY PANEL

    Foam Hand Sanitizer

    with Moisturizers

    1000 mL (33.8 FL OZ)

    container labelb

    container label

  • INGREDIENTS AND APPEARANCE
    ENMOTION FOAM HAND SANITIZER 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54622-120
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POTASSIUM HYDROLYZED JOJOBA ESTERS (UNII: CH428W5O62)  
    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)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54622-120-012 in 1 BOX01/25/2018
    11000 mL in 1 BAG; Type 0: Not a Combination Product
    2NDC:54622-120-022 in 1 BOX01/25/2018
    21000 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/25/2018
    Labeler - Georgia-Pacific Consumer Products LP (806142217)
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