DR.DAVEY 75% ALCOHOL WIPES- alcohol cloth

Dr.Davey 75% alcohol wipes by

Drug Labeling and Warnings

Dr.Davey 75% alcohol wipes by is a Otc medication manufactured, distributed, or labeled by SHANTOU S.E.Z BAOJIE INDUSTRY CO., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

If redness or irritation develop and persist for more than 72 hours

DO NO USE AROUND EYES. DO NOT USE IN EARS AND MOUTH

for personal hand hygiene to helo prevent the spread of bacteria kills harmful bacteria or germs

AVOID CONTACT WITH EYES. IN CASE OF CONTACT FLUSH EYES WITH WATER.CHILDREN MUST BE SUPERVISED IN USE THIS PRODUCT

water, benzalkonium chloride

ethyl alcohol

for occasional and personal domestic use rub throughly into hands for at least 30 seconds. allow to dry

Store at20℃ may discolor fabrics

Antiseptic, alcohol wipes

bag

INGREDIENTS AND APPEARANCE

DR.DAVEY 75% ALCOHOL WIPES 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74913-900
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 U

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)	0.03 mL  in 100 U
WATER (UNII: 059QF0KO0R)	24.97 mL  in 100 U

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74913-900-01	100 U in 1 BAG; Type 0: Not a Combination Product	06/01/2020
2	NDC: 74913-900-02	50 U in 1 BAG; Type 0: Not a Combination Product	06/01/2020
3	NDC: 74913-900-03	80 U in 1 BAG; Type 0: Not a Combination Product	06/01/2020
4	NDC: 74913-900-04	100 U in 1 BOX; Type 0: Not a Combination Product	06/01/2020
5	NDC: 74913-900-05	50 U in 1 BOX; Type 0: Not a Combination Product	06/01/2020
6	NDC: 74913-900-06	80 U in 1 BOX; Type 0: Not a Combination Product	06/01/2020
7	NDC: 74913-900-07	80 U in 1 JAR; Type 0: Not a Combination Product	06/01/2020
8	NDC: 74913-900-09	120 U in 1 JAR; Type 0: Not a Combination Product	06/01/2020
9	NDC: 74913-900-08	20 U in 1 BAG; Type 0: Not a Combination Product	06/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/01/2020

Labeler - SHANTOU S.E.Z BAOJIE INDUSTRY CO., LTD (546345856)

Registrant - SHANTOU S.E.Z BAOJIE INDUSTRY CO., LTD (546345856)

Establishment
Name	Address	ID/FEI	Business Operations
SHANTOU S.E.Z BAOJIE INDUSTRY CO., LTD		546345856	manufacture(74913-900)