DISINFECTANT LIQUID ANTIBACTERIAL- disinfectant liquid antibacterial spray spray

Disinfectant liquid Antibacterial by

Drug Labeling and Warnings

Disinfectant liquid Antibacterial by is a Otc medication manufactured, distributed, or labeled by Guangzhou Dedo Pharmaceutical Co.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

HYPOCHLOROUS ACID 0.02%

Purpose

DISINFECTANT LIQUID

Use

SUITABLE FOR GENERAL OBJECT SURFACE,SKIN SURFACE,VEGETABLE AND FRUIT DISINFECTION ETC.EFFECTIVELY INHIBIT STAPHYLOCOCCUS AUREUS,CANDIDA ALBICANS AND ESCHERICHIA COLI.

Warnings

for external use only.

DO NOT USE

WHEN USING

do not use in or near the eyes.In case of contact.rinse eyes thoroughly with water.Stop use and ask doctor if irritation or rash appears and lasts.

Keep out of teach for children.

If swallowed,get medical help or contact a Poison Control Center right away.

STOP USE

KEEP OUT OF REACH OF CHILDREN

Directions

GENERAL OBJECT AND SKIN DISINFECTION:DIRECT SPRAYING OF PRODUCTS ON GENERAL OBJECTS OR SKIN SURFACES REQUIRING DISINFECTION;FRUITS AND VEGETABLES DISINFECTION:SPRAY DIRECTLY ON THE FRUIT AND VEGETABLE SURFACE AND FINSE WITH WATER AFTER 10 MINUTES

Children under 6 years of age should be supervised when using this product.

Other information

Please keep it in a cool and ventilated place.DO NOT MIX WITH OTHER PRODUCTS OR WATER.

Inactive ingredients

Water(Aqua),SODIUM CHLORIDE

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

DISINFECTANT LIQUID ANTIBACTERIAL 
disinfectant liquid antibacterial spray spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74534-014
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 g

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74534-014-01	500 g in 1 BOTTLE; Type 0: Not a Combination Product	04/13/2020
2	NDC: 74534-014-12	600 g in 1 BOTTLE; Type 0: Not a Combination Product	04/13/2020
3	NDC: 74534-014-02	300 g in 1 BOTTLE; Type 0: Not a Combination Product	04/13/2020
4	NDC: 74534-014-03	200 g in 1 BOTTLE; Type 0: Not a Combination Product	04/13/2020
5	NDC: 74534-014-04	100 g in 1 BOTTLE; Type 0: Not a Combination Product	04/13/2020
6	NDC: 74534-014-05	120 g in 1 BOTTLE; Type 0: Not a Combination Product	04/13/2020
7	NDC: 74534-014-07	1000000 g in 1 BOTTLE; Type 0: Not a Combination Product	04/13/2020
8	NDC: 74534-014-06	250 g in 1 BOTTLE; Type 0: Not a Combination Product	04/13/2020
9	NDC: 74534-014-08	100000 g in 1 BOTTLE; Type 0: Not a Combination Product	04/13/2020
10	NDC: 74534-014-09	50000 g in 1 BOTTLE; Type 0: Not a Combination Product	04/13/2020
11	NDC: 74534-014-10	2000 g in 1 BOTTLE; Type 0: Not a Combination Product	04/13/2020
12	NDC: 74534-014-11	1000 g in 1 BOTTLE; Type 0: Not a Combination Product	04/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/13/2020

Labeler - Guangzhou Dedo Pharmaceutical Co.,Ltd (418394705)

Registrant - Guangzhou Dedo Pharmaceutical Co.,Ltd (418394705)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Dedo Pharmaceutical Co.,Ltd		418394705	manufacture(74534-014)