Label: DR.BETTER HOMES 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 January 21, 2021

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  • Active Ingredient

    Ethanol 70%

  • Purpose

    Antiseptic

  • Uses

    To help reduce bacteria on the skin

  • Warnings

    For external use only.

    Flammable, keep away from heat or flames.

  • When using this product

    keep away from eyes. In case of eye contact, rinse eyes with water.

  • Stop use and ask doctor if

    irritation and redness develop and persist.

  • Keep out of reach of children.

  • Directions

    Apply a small amount in your palm and rub hands together briskly until dry.

    Supervise children under 6 years in the use of product.

  • Other Information

    Protect this product from excessive heat and direct sun.

  • Inactive Ingredients

    Glycerin, Sodium Hyaluronate, Carbomer, Butylene Glycol, Aloe Extract, Triethanolamine, Flavoring, Purified Water

  • Package Label

    75615-0020-0 10000ml

    75615-0020-1 500ml

    75615-0020-2 50ml

    75615-0020-3 60ml

    75615-0020-4 100ml

    75615-0020-5 200ml

    75615-0020-6 250ml

    75615-0020-7 300ml

    75615-0020-8 5000ml

    75615-0020-9 3785ml

  • INGREDIENTS AND APPEARANCE
    DR.BETTER HOMES HAND SANITIZER 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75615-0020
    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
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK)  
    WATER (UNII: 059QF0KO0R)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    ALOE (UNII: V5VD430YW9)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75615-0020-1500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/08/2020
    2NDC:75615-0020-250 mL in 1 BOTTLE; Type 0: Not a Combination Product05/21/2020
    3NDC:75615-0020-360 mL in 1 BOTTLE; Type 0: Not a Combination Product05/21/2020
    4NDC:75615-0020-4100 mL in 1 BOTTLE; Type 0: Not a Combination Product05/21/2020
    5NDC:75615-0020-5200 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/21/2020
    6NDC:75615-0020-6250 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/21/2020
    7NDC:75615-0020-7300 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/21/2020
    8NDC:75615-0020-85000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/26/2020
    9NDC:75615-0020-93785 mL in 1 BOTTLE; Type 0: Not a Combination Product07/22/2020
    10NDC:75615-0020-010000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product07/22/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/08/2020
    Labeler - UI COSMETICS CO., LTD (688362189)
    Registrant - UI COSMETICS CO., LTD (688362189)
    Establishment
    NameAddressID/FEIBusiness Operations
    UI COSMETICS CO., LTD688362189manufacture(75615-0020)
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