Label: HANNA DISINFECTANTSPRAY- sodium hypochlorite liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated June 13, 2020

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  • ACTIVE INGREDIENT

    sodium hypochlorite

  • INACTIVE INGREDIENT

    WATER, peg-60 hydrogenated castor oil, aloe extract, camellia sinensis leaf extract, grapefruit seed extract, fragrance

  • PURPOSE

    Sterilization of hands and skin

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF THE CHILDREN

  • INDICATIONS & USAGE

    Apply an appropriate amount on your hands and rub well to dry.

  • WARNINGS

    1. Do not use on the following body parts. A wide range of body parts and damaged skin around the eyes and ears, in the oral cavity (may have irritating effects)
    2. If the following symptoms appear, stop using them immediately and consult a doctor or pharmacist.
    1) Hypersensitivity symptoms such as rash, erythema, itching, and edema
    2) Skin irritation symptoms

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    HANNA DISINFECTANTSPRAY 
    sodium hypochlorite liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74247-0014
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM HYPOCHLORITE (UNII: DY38VHM5OD) (HYPOCHLORITE ION - UNII:T5UM7HB19N) SODIUM HYPOCHLORITE0.02 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    GRAPEFRUIT PEEL (UNII: 3582N05Q44)  
    PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74247-0014-155 mL in 1 BOTTLE; Type 0: Not a Combination Product06/13/2020
    2NDC:74247-0014-2300 mL in 1 BOTTLE; Type 0: Not a Combination Product06/13/2020
    3NDC:74247-0014-3500 mL in 1 BOTTLE; Type 0: Not a Combination Product06/13/2020
    4NDC:74247-0014-42000 mL in 1 BOTTLE; Type 0: Not a Combination Product06/13/2020
    5NDC:74247-0014-55000 mL in 1 BOTTLE; Type 0: Not a Combination Product06/13/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/13/2020
    Labeler - Rainbow Co Ltd (690423720)
    Registrant - Rainbow Co Ltd (690423720)
    Establishment
    NameAddressID/FEIBusiness Operations
    Rainbow Co Ltd690423720manufacture(74247-0014)
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