Label: SNUGZ HAND SANITIZER GEL- hand sanitizer gel gel

  • NDC Code(s): 76309-301-01, 76309-301-02, 76309-301-04, 76309-301-05, view more
    76309-301-08, 76309-301-19, 76309-301-51, 76309-301-61, 76309-301-62, 76309-301-81, 76309-301-88, 76309-301-91, 76309-301-99
  • Packager: SnugZ/USA, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 31, 2023

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  • DOSAGE & ADMINISTRATION

    Wet hands thoroughly with product and rub into skin until dry.

  • WARNINGS

    Warnings: For external use only. Flammable, keep away from fire. Do not use on damaged or broken skin. Keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs. Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

  • INACTIVE INGREDIENT

    Inactive Ingredients: Aminomethyl Propanol, Carbomer, Water

  • ACTIVE INGREDIENT

    Active Ingredients: Ethyl Alcohol 70% v/v

  • PURPOSE

    Purpose: Antiseptic

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • INDICATIONS & USAGE

    Indications: Helps reduce bacteria on skin.

  • Hand Sanitizer Gel

    ZS10-UNSC

  • INGREDIENTS AND APPEARANCE
    SNUGZ HAND SANITIZER GEL 
    hand sanitizer gel gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76309-301
    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
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76309-301-0128 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2018
    2NDC:76309-301-0256 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2018
    3NDC:76309-301-04112 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2018
    4NDC:76309-301-08224 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/01/2018
    5NDC:76309-301-1956 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2018
    6NDC:76309-301-5130 mL in 1 TUBE; Type 0: Not a Combination Product01/01/2018
    7NDC:76309-301-0514 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2018
    8NDC:76309-301-8128 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2018
    9NDC:76309-301-9128 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2018
    10NDC:76309-301-6139.75 mL in 1 POUCH; Type 0: Not a Combination Product01/01/2018
    11NDC:76309-301-6285.17 mL in 1 POUCH; Type 0: Not a Combination Product01/01/201812/31/2020
    12NDC:76309-301-993785.41 mL in 1 JUG; Type 0: Not a Combination Product04/20/2020
    13NDC:76309-301-88112 mL in 1 POUCH; Type 0: Not a Combination Product04/20/202012/31/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/01/2018
    Labeler - SnugZ/USA, LLC (615959228)
    Registrant - SnugZ/USA, LLC (615959228)
    Establishment
    NameAddressID/FEIBusiness Operations
    SnugZ/USA, LLC615959228manufacture(76309-301)
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