Label: CLEAN CARE HAND SANITIZER- alcohol gel

  • Category: HUMAN OTC DRUG LABEL

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 April 2, 2020

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  • ACTIVE INGREDIENT

    ethyl alcohol

  • PURPOSE

    The convenient Sense Fresh Advanced Instant Hand Sanitizer with Aloe is an antimicrobial liquid that contains 70 percent ethyl alcohol to help reduce the number of germs on hands, and three moisturizers to help keep skin hydrated. No rinsing with water or drying with towels is needed. Alcohol-based hand sanitizers can quickly reduce the number of germs on hands within 30 seconds. The hand sanitizer meets U.S. Food and Drug Administration (FDA) healthcare personnel hand-washing requirements. It’s perfect for on-the-go uses when traveling outside of the home, and fits neatly in purses, backpacks or briefcases.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF THE CHILDREN

  • INDICATIONS & USAGE

    Just spray enough product in your palm to cover hands and rub hands together briskly until dry.

    Children under 6 years of age should be supervised when using Sense Fresh.

    Hand sanitizer to help reduce bacteria on the skin that could cause disease. Recommended for repeated use.

  • WARNINGS

    ■ Flammable. Keep away from fire or flame.

    ■ For external use only.

    ■ Do not use in eyes.

    ■ lf swallowed, get medical help promptly.

    ■ Stop use, ask doctor lf irritation occurs.

    ■ Keep out of reach of children.

  • DOSAGE & ADMINISTRATION

    for external use only

  • INACTIVE INGREDIENT

    water, trolamine, dipropylene glycol, carbomer

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    CLEAN CARE HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74200-0002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74200-0002-1500 mL in 1 BOTTLE; Type 0: Not a Combination Product04/01/2020
    2NDC:74200-0002-2100 mL in 1 BOTTLE; Type 0: Not a Combination Product04/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/01/2020
    Labeler - URBANBCL CO LTD (694794065)
    Registrant - URBANBCL CO LTD (694794065)
    Establishment
    NameAddressID/FEIBusiness Operations
    URBANBCL CO LTD694794065manufacture(74200-0002)
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