DISINFECTANT LIQUID ANTIBACTERIAL- disinfectant liquid antibacterial spray spray 
Guangzhou Dedo Pharmaceutical Co.,Ltd

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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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 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.

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

ALL

DISINFECTANT LIQUID ANTIBACTERIAL 
disinfectant liquid antibacterial spray spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74534-014
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYPOCHLOROUS ACID (UNII: 712K4CDC10) (HYPOCHLOROUS ACID - UNII:712K4CDC10) HYPOCHLOROUS ACID0.02 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:74534-014-01500 g in 1 BOTTLE; Type 0: Not a Combination Product04/13/2020
2NDC:74534-014-12600 g in 1 BOTTLE; Type 0: Not a Combination Product04/13/2020
3NDC:74534-014-02300 g in 1 BOTTLE; Type 0: Not a Combination Product04/13/2020
4NDC:74534-014-03200 g in 1 BOTTLE; Type 0: Not a Combination Product04/13/2020
5NDC:74534-014-04100 g in 1 BOTTLE; Type 0: Not a Combination Product04/13/2020
6NDC:74534-014-05120 g in 1 BOTTLE; Type 0: Not a Combination Product04/13/2020
7NDC:74534-014-071000000 g in 1 BOTTLE; Type 0: Not a Combination Product04/13/2020
8NDC:74534-014-06250 g in 1 BOTTLE; Type 0: Not a Combination Product04/13/2020
9NDC:74534-014-08100000 g in 1 BOTTLE; Type 0: Not a Combination Product04/13/2020
10NDC:74534-014-0950000 g in 1 BOTTLE; Type 0: Not a Combination Product04/13/2020
11NDC:74534-014-102000 g in 1 BOTTLE; Type 0: Not a Combination Product04/13/2020
12NDC:74534-014-111000 g in 1 BOTTLE; Type 0: Not a Combination Product04/13/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other04/13/2020
Labeler - Guangzhou Dedo Pharmaceutical Co.,Ltd (418394705)
Registrant - Guangzhou Dedo Pharmaceutical Co.,Ltd (418394705)
Establishment
NameAddressID/FEIBusiness Operations
Guangzhou Dedo Pharmaceutical Co.,Ltd418394705manufacture(74534-014)

Revised: 4/2020
Document Id: a414e089-0fcb-5f61-e053-2995a90aa47c
Set id: a414fdf3-63c9-1f1d-e053-2995a90a66d9
Version: 4
Effective Time: 20200424
 
Guangzhou Dedo Pharmaceutical Co.,Ltd