Label: DMS COALITION HAND SANITIZER- ethanol 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 July 13, 2020

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient

    Alcohol 70%

  • PURPOSE

    Purpose
    Antiseptic

  • INDICATIONS & USAGE

    Uses

    • to decrease bacteria on the skin
    • recommended for repeated use
  • WARNINGS

    Warnings
    For external use only.
    Flammable. Keep away from fire or flame.

    When using this product keep away from eyes. In case of eye contact, rinse eyes with water.

    Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.

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

  • DOSAGE & ADMINISTRATION

    Directions

    • apply liberally to hands to cover all surfaces
    • rub hands together until dry
    • supervise children under 6 years old
    • not recommended for infants
  • STORAGE AND HANDLING

    Other information

    store below 43°C (109.4°F)

  • INACTIVE INGREDIENT

    Inactive ingredients

    Purified water, Glycerin, Hydroxypropyl Methylcellulose, Fragrance

  • SPL UNCLASSIFIED SECTION

    Distributed by:
    dms COALITION | DOMESTIC MEDICAL SUPPLY
    400 Continental Blvd. Fl 6
    El Segundo, CA 90245

  • PRINCIPAL DISPLAY PANEL

    dms COALITION | DOMESTIC MEDICAL SUPPLY
    ADVANCED HAND SANITIZER

    TOPICAL SOLUTION
    ALCOHOL ANTISEPTIC 70%
    NON-STERILE SOLUTION

    Kills 99.99% of germs and bacteria
    RAPID ACTION
    2 FL OZ (59 mL)
    CITRUS SCENT

    DMSC-HS-Scent Final

  • INGREDIENTS AND APPEARANCE
    DMS COALITION HAND SANITIZER 
    ethanol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79407-002
    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
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79407-002-16500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/13/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E07/13/2020
    Labeler - Domestic Medical Supply Coalition, LLC (117476381)
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