Label: SCOTT GEL HAND SANITIZER WITH MOISTURIZERS- ethyl alcohol gel

  • 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 July 22, 2021

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Ethyl Alcohol 62.5% v/v.

  • Purposes

    Antiseptic cleanser

  • Uses

    to decrease potentially harmful germs on skin.

  • Warnings

    For external use only

    Flammable, keep away from fire or flame, heat, sparks, and sources of static discharge

    Do not use

    In eyes

    When using this product

    If in eyes, rinse promplty and thoroughly with water. Discontinue use if irritation and redness develop.

    Stop use and ask a doctor if skin irritation or redness occurs or 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

    Apply product onto hands, spread thoroughly and rub dry.

  • Other information

    Report serious side effects from this product to 1-877-561-6587. Do not store above 104°F (40°C).

  • Inactive Ingredients

    Water (Aqua), Propylene Glycol, Dimethicone PEG-7 Isostearate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethylpropanediol, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice.

  • Questions?

    1-888-346-4652

  • PRINCIPAL DISPLAY PANEL - 946 mL Bottle Label

    53458

    Scott®
    Brand

    Gel Hand Sanitizer
    with Moisturizers

    KILLS UP TO
    99.99%
    OF GERMS

    32 oz (946 mL)

    PRINCIPAL DISPLAY PANEL - 946 mL Bottle Label
  • INGREDIENTS AND APPEARANCE
    SCOTT GEL HAND SANITIZER WITH MOISTURIZERS 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55118-702
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62.5 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    DIMETHICONE PEG-7 ISOSTEARATE (UNII: JVS3399FNW)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55118-702-30946 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E05/15/2020
    Labeler - Kimberly-Clark (830997032)
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