HANNA DISINFECTANTSPRAY- sodium hypochlorite liquid 
Rainbow Co Ltd

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Drug Facts

sodium hypochlorite

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

Sterilization of hands and skin

KEEP OUT OF REACH OF THE CHILDREN

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

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

for external use only

label

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)

Revised: 6/2020
Document Id: a7ee61ef-1c6f-ae55-e053-2a95a90af643
Set id: a7ee6281-8fda-7a28-e053-2995a90a05fd
Version: 1
Effective Time: 20200613
 
Rainbow Co Ltd