HANNA DISINFECTANTSPRAY- sodium hypochlorite liquid

HANNA DISINFECTANTspray by

Drug Labeling and Warnings

HANNA DISINFECTANTspray by is a Otc medication manufactured, distributed, or labeled by Rainbow Co Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

HANNA DISINFECTANTSPRAY 
sodium hypochlorite liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74247-0014
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM HYPOCHLORITE (UNII: DY38VHM5OD) (HYPOCHLORITE ION - UNII:T5UM7HB19N)	SODIUM HYPOCHLORITE	0.02 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74247-0014-1	55 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/13/2020
2	NDC: 74247-0014-2	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/13/2020
3	NDC: 74247-0014-3	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/13/2020
4	NDC: 74247-0014-4	2000 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/13/2020
5	NDC: 74247-0014-5	5000 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/13/2020

Labeler - Rainbow Co Ltd (690423720)

Registrant - Rainbow Co Ltd (690423720)

Establishment
Name	Address	ID/FEI	Business Operations
Rainbow Co Ltd		690423720	manufacture(74247-0014)