SHIERJIE HYPOCHLOROUS ACID- hypochlorous acid liquid

Shierjie Hypochlorous Acid by

Drug Labeling and Warnings

Shierjie Hypochlorous Acid by is a Otc medication manufactured, distributed, or labeled by Shenzhen Shierjie Biological Engineering Co., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Hypochlorous acid 0.02%

Purpose

Antiseptic, antiseptic

Use

Used to wash hands to help reduce bacteria that potentiallycancause disease

Warnings

For external use only. Keep away from heat

Do not use

1.In children less than 2 months ofage.

2. On open skin wounds

When Using

do not use in ornear the eyes,in case ofcontact, rinse eyes thoroughly with water.

Stop Use

Stop use and ask doctor if irritationor rash appears and lasts. Keep out of reach for children.lf swallowed, getmedical help or contact a Poison Control Center right away.

Ask Doctor

ask doctor if irritationor rash appears and lasts. Keep out of reach for children.lf swallowed, getmedical help or contact a Poison Control Center right away.

Keep Oot Of Reach Of Children

Supervise children under 6 years of age when usingthis productto avoid
swallowing.

Directions

Place enough product on hands to cover all surfaces.Rub hands together unti dry.Supervise children under 6 years of age when usingthis productto avoid
swallowing.

Other information

Store between 13-30°C. Avoid freezing and excessive heat above 40°C.

Inactive ingredients

Sodium Chloride (Salt), Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SHIERJIE HYPOCHLOROUS ACID 
hypochlorous acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43116-032
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10)	HYPOCHLOROUS ACID	0.02 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43116-032-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/19/2023
2	NDC: 43116-032-02	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/19/2023
3	NDC: 43116-032-03	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/19/2023
4	NDC: 43116-032-04	300 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/19/2023
5	NDC: 43116-032-05	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/19/2023
6	NDC: 43116-032-06	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/19/2023
7	NDC: 43116-032-07	2500 mL in 1 PAIL; Type 0: Not a Combination Product	11/19/2023
8	NDC: 43116-032-08	5000 mL in 1 PAIL; Type 0: Not a Combination Product	11/19/2023
9	NDC: 43116-032-09	20000 mL in 1 PAIL; Type 0: Not a Combination Product	11/19/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	11/19/2023

Labeler - Shenzhen Shierjie Biological Engineering Co., LTD (547610261)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Shierjie Biological Engineering Co., LTD		547610261	manufacture(43116-032)