Label: ENMOTION FOAM HIGH FREQUENCY USE- ethyl alcohol solution

  • NDC Code(s): 54622-121-01
  • 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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  • 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

    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, Chamomilla Recutita (Matricaria) Flower Extract, Camellia Sinensis Leaf Extract, Avena Sativa (Oat) Kernel Extract, Euterpe Oleracea Fruit Extract, Butylene Glycol, Bisabolol, Phenoxyethanol, Citric Acid, Sodium Benzoate, Potassium Sorbate, Acetyl Hexapeptide-49

    *may contain this ingredient

  • Rear label text

    enMotion

    High Frequency Use

    Foam Hand Sanitizer

    Fragrance Free SKU 42336

    Manufactured for

    Georgia-Pacific Consumer Products. Atlanta, GA 30303

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

    or visit us online at www.gppro.com

    (c) 2021 GP PRO. All rights reserved.

    alcohol permit SDS-KY-15002

    5000008656/000/02

  • principal display panel

    High Frequency Use

    Foam Hand Sanitizer

    1000 mL (33.8 FL OZ)

    container label

    container labelb

  • INGREDIENTS AND APPEARANCE
    ENMOTION FOAM  HIGH FREQUENCY USE
    ethyl alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54622-121
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  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)  
    GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER)  
    CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17)  
    AVENA SATIVA WHOLE (UNII: 5P8D0Z74RG)  
    EUTERPE OLERACEA WHOLE (UNII: Y57H6218HP)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    .BETA.-BISABOLOL (UNII: LP618AV2EA)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    ACETYL HEXAPEPTIDE-49 (UNII: 4055X1S509)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54622-121-012 in 1 BOX06/10/2021
    11000 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)06/10/2021
    Labeler - Georgia-Pacific Consumer Products LP (806142217)
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