Label: SHIMMY ORIGINAL HAND SANITIZER- alcohol spray

  • NDC Code(s): 81755-001-92, 81755-001-93
  • Packager: Shimmy Products LLC
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated July 25, 2024

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  • Active Ingredients

    Ethyl Alcohol 70% v/v

  • Purpose

    Antimicrobial

  • Uses

    • hand sanitizer to help reduce bacteria on the skin that could cause disease.
    • for use when soap and water are not available
  • Warnings

    For external use only.

    Flammable. Keep away from heat or flame.

  • Do not use

    • on children less than 2 months of age
    • on open skin wounds
  • When using this product

    • keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

  • Stop use and ask a doctor

    if irritation or rash appears or lasts. These may be signs of a serious condition.

  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Put enough product in your palm to cover your hands and rub hands together briskly until dry
    • Children under 6 years of age should be supervised when using this product.
  • Other information

    • Avoid freezing and excessive heat above 40ºC (104ºF).
    • May discolor certain fabrics, materials or surfaces.
  • Inactive ingredients

    water, glycerin, aloe barbadensis leaf juice, carbomer, sodium hydroxide, fragrance

  • Package Label - Principal Display Panel

    SHIMMY ORIGINAL HAND SANITIZER

    8 fl oz (236 mL)

    NDC: 81755-001-92

    SH25600E

    SHIMMY ORIGINAL HAND SANITIZER

    9 fl oz (266 mL)

    NDC: 81755-001-93

    SH25603E

  • INGREDIENTS AND APPEARANCE
    SHIMMY ORIGINAL HAND SANITIZER 
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81755-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81755-001-92236 mL in 1 CAN; Type 0: Not a Combination Product06/14/2021
    2NDC:81755-001-93266 mL in 1 CAN; Type 0: Not a Combination Product06/14/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/14/2021
    Labeler - Shimmy Products LLC (117838009)
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