STERILIZED WET WIPES cloth

Sterilized Wet Wipes by

Drug Labeling and Warnings

Sterilized Wet Wipes by is a Otc medication manufactured, distributed, or labeled by ZHEJIANG BAOJIA BIOTECHNOLOGY CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient(s)

Benzalkonium Chloride 0.1%,DDAC 0.1%

Purpose

Antiseptic

Use(s)

Health care personnel hand rub to help reduce bacteria that potentially can cause diseaze.

Warnings

For extemal use only, Avoid extreme temperature

Do not use

In children less than 6 months of age

On open skin wounds

When using this product

Keep out of eyes and mouth, in case of contact with eyes,rinse eyes thoroughly with water.

Stop use and ask a doctor

lf iirritation or rash occurs, these may be signs of a serious condition.

Keep out of the reach of children

if swallowed,get a medical help or call a poison control center right away.

Directions

pull out the wipes to rub all surfaces of hands,.

Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

Store between 5-30℃(41-86F)

Avoid freezing and excessive heat above 40(104F)

Inactive ingredients

Glycerin, Phenoxyethanol Ethylhexylglycerin, Propylene Glycol,Purfied Water.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

STERILIZED WET WIPES 
sterilized wet wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78447-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B) (DIDECYLDIMONIUM - UNII:Z7F472XQPA)	DIDECYLDIMONIUM CHLORIDE	0.1 g  in 100 mL
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78447-002-01	6 mL in 1 BAG; Type 0: Not a Combination Product	06/08/2020
2	NDC: 78447-002-02	30 mL in 1 BAG; Type 0: Not a Combination Product	06/08/2020
3	NDC: 78447-002-03	60 mL in 1 BAG; Type 0: Not a Combination Product	06/08/2020
4	NDC: 78447-002-04	90 mL in 1 BAG; Type 0: Not a Combination Product	06/08/2020
5	NDC: 78447-002-05	170 mL in 1 BAG; Type 0: Not a Combination Product	06/08/2020
6	NDC: 78447-002-06	240 mL in 1 BAG; Type 0: Not a Combination Product	06/08/2020
7	NDC: 78447-002-07	300 mL in 1 BAG; Type 0: Not a Combination Product	06/08/2020
8	NDC: 78447-002-08	570 mL in 1 BAG; Type 0: Not a Combination Product	06/08/2020
9	NDC: 78447-002-09	600 mL in 1 BAG; Type 0: Not a Combination Product	06/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/08/2020

Labeler - ZHEJIANG BAOJIA BIOTECHNOLOGY CO., LTD. (421280658)

Registrant - ZHEJIANG BAOJIA BIOTECHNOLOGY CO., LTD. (421280658)

Establishment
Name	Address	ID/FEI	Business Operations
ZHEJIANG BAOJIA BIOTECHNOLOGY CO., LTD.		421280658	manufacture(78447-002)