Label: ECOLAB- alcohol solution

  • NDC Code(s): 47593-487-26, 47593-487-31, 47593-487-33, 47593-487-49, view more
    47593-487-55
  • Packager: Ecolab Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 10/13

If you are a consumer or patient please visit this version.

  • Active ingredient

    Ethyl Alcohol 70% w/w

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  • Purpose

    Antiseptic handwash

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  • Uses

    • For handwashing to decrease bacteria on skin
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  • 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 promptly and thoroughly with water
    • Discontinue use if irritation and redness develop

    Stop use and ask a doctor if

    • Skin irritation or redness occurs for more than 72 hours

    ​Keep out of reach of children.​ If swallowed, get medical help or contact a Poison Control Center right away.

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  • Directions

    • Apply product onto hands, spread thoroughly and rub until dry
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  • Other information

    • for additional information, see Material Safety Data Sheet (MSDS)
    • for emergency medical information in USA, call 1 800 328 0026
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  • INACTIVE INGREDIENT

    ​Inactive ingredients​ water (aqua), isopropyl alcohol, carbomer, propylene glycol, tert-butyl alcohol, aminomethyl propanol, fragrance, denatonium benzoate.

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  • QUESTIONS

    ​Questions? ​call ​1 866 781 8787

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  • Representative Label and Principal Display Panel

    ECOLAB

    NDC 47593-487-26

    Gel Hand Sanitizer

    Active Ingredient:  70% Ethyl Alcohol

    6030349

    Net Contents:  1000 mL (33.8 fl oz)

    752032/8500/0912

    representative labelrepresentative label

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  • INGREDIENTS AND APPEARANCE
    ECOLAB 
    alcohol solution
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:47593-487
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (ALCOHOL) ALCOHOL 589.4 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    ISOPROPYL ALCOHOL  
    CARBOMER INTERPOLYMER TYPE A (55000 CPS)  
    PROPYLENE GLYCOL  
    TERT-BUTYL ALCOHOL  
    AMINOMETHYLPROPANOL  
    DENATONIUM BENZOATE  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:47593-487-33 118 mL in 1 BOTTLE, PLASTIC
    2 NDC:47593-487-31 540 mL in 1 BOTTLE, PLASTIC
    3 NDC:47593-487-26 1000 mL in 1 POUCH
    4 NDC:47593-487-49 37 mL in 1 BOTTLE, PLASTIC
    5 NDC:47593-487-55 1000 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333E 11/28/2012
    Labeler - Ecolab Inc. (006154611)
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