MEDIBLUE- hypochlorous acid liquid

MEDIBLUE by

Drug Labeling and Warnings

MEDIBLUE by is a Otc medication manufactured, distributed, or labeled by Multibio Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Hypochlorous acid 0.005%

PURPOSE

Antiseptic

USES

Multi purpose sterilization, disinfection

WARNINGS

For external use only

WHEN USING THIS PRODUCT

Keep out of eyes, in case of contact with eyes, flush thoroughly with water

Avoid contact with broken skin

Do not inhale or ingest

WHEN USING THIS PRODUCT

Stop immediately and consult a doctor it you experience skin imitation or rash develops

WHEN USING THIS PRODUCT

Keep out of reach of children. if swallowed, get medical help or contact a posion control center right away.

DIRECTIONS

Spray the sterilizing object in a wide range

Please supervise when using the product by children, the elderly, the disabled, etc.

OTHER INFORMATION

Read the directions and warnings before use

If exposed to the air, sterilization may be reduced due to water-soluble, so keep the container sealed.

Avoid freezing and excessive heat above 40 degree C (104 degree F) 40C(104F)

INACTIVE INGREDIENTS

Water

PACKAGE LABEL

INGREDIENTS AND APPEARANCE

MEDIBLUE 
hypochlorous acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76847-301
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10)	HYPOCHLOROUS ACID	0.005 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	99.995 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76847-301-01	500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/27/2020
2	NDC: 76847-301-02	4000 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/27/2020
3	NDC: 76847-301-03	20000 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/27/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/27/2020

Labeler - Multibio Co., Ltd (693713128)

Registrant - Multibio Co., Ltd (693713128)

Establishment
Name	Address	ID/FEI	Business Operations
Multibio Co., Ltd		693713128	manufacture(76847-301)