SUFIYA (hocl- hypochlorous acid liquid

Sufiya by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredient[s]

HOCl (Hypochlorous acid) 0.1%

Purpose

Disinfect, deodorization

Use[s]

Sanitizer and disinfectant to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame

Do not use

• for any other purpose
• in children less than 2 months of ago
• on open skin wounds

When using this product

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

if any abnormality occurs on the skin.

Keep out of reach of children.

If swallowed, drink enough water and get medical help or contact a Poison Control Center right away.

Directions

• Spray from a distance of 4-8 inches where sterilization, disinfection, and deodorization are required
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 15-30C(58-86F)
• Avoid freezing and excessive heat above 40C(104F)
• If medical treatment is required, look at the product container or labeling information.

Inactive ingredients

Purified water

Package Label

INGREDIENTS AND APPEARANCE

SUFIYA 
hocl(hypochlorous acid) liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82124-701
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10)	HYPOCHLOROUS ACID	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82124-701-01	60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/20/2021
2	NDC: 82124-701-02	600 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/20/2021
3	NDC: 82124-701-03	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/20/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/20/2021

Labeler - EMSOLUTION Co., Ltd (694603987)

Registrant - EMSOLUTION Co., Ltd (694603987)

Establishment
Name	Address	ID/FEI	Business Operations
EMSOLUTION Co., Ltd		694603987	manufacture(82124-701)