WET WIPES- benzalkonium chloride,didecyldimonium chloride swab

Wet wipes by

Drug Labeling and Warnings

Wet wipes by is a Otc medication manufactured, distributed, or labeled by Hangzhou LUC Travel Products Co., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Didecyldimonium Chloride 0.2%..

Benzalkonium Chloride 0.1%

Purpose

Germicidal

USE

For decrease bacteria on skin

Warning

For external use only
■Do not use if you are allergic to any of these ingredients
When using this products do not get into eyes
If contact occurs, rinse thorough with water

■ Keep out of reach of children unless under adult
supervision. If swallowe, get medical help or contact
a Poison Control Center immediately

Directions

Thoroughly wipes hands or face with wipes. Discard in
trash receptacle
■Do not flush. Dispose of in rubbish after use
1 I Store in cool dry place, away from heat and direct
sunlight

Inactive ingredients

Aqua, DecyI Glucoside, Phenoxyethanol, Didecyldimonium
Chloride, Polysorbate 20, Aloe Barbadensis Leaf Juice,
Benzalkonium Chloride, Disodium EDTA

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

WET WIPES 
benzalkonium chloride,didecyldimonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75213-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B) (DIDECYLDIMONIUM - UNII:Z7F472XQPA)	DIDECYLDIMONIUM CHLORIDE	0.2 g  in 100 g
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75213-001-01	100 in 1 CARTON	03/21/2020
1		10 in 1 BAG
1		0.036 g in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 75213-001-02	100 in 1 CARTON	03/21/2020
2		25 in 1 BAG
2		0.09 g in 1 POUCH; Type 0: Not a Combination Product
3	NDC: 75213-001-03	24 in 1 CARTON	03/21/2020
3		50 in 1 BAG
3		0.18 g in 1 POUCH; Type 0: Not a Combination Product
4	NDC: 75213-001-04	12 in 1 CARTON	03/21/2020
4		100 in 1 BAG
4		0.36 g in 1 POUCH; Type 0: Not a Combination Product
5	NDC: 75213-001-05	12 in 1 CARTON	03/21/2020
5		75 in 1 BAG
5		0.216 g in 1 POUCH; Type 0: Not a Combination Product
6	NDC: 75213-001-06	12 in 1 CARTON	03/21/2020
6		60 in 1 PAIL
6		0.216 g in 1 POUCH; Type 0: Not a Combination Product
7	NDC: 75213-001-07	12 in 1 CARTON	03/21/2020
7		75 in 1 PAIL
7		0.27 g in 1 POUCH; Type 0: Not a Combination Product
8	NDC: 75213-001-08	12 in 1 CARTON	03/21/2020
8		80 in 1 PAIL
8		0.288 g in 1 POUCH; Type 0: Not a Combination Product
9	NDC: 75213-001-09	12 in 1 CARTON	03/21/2020
9		100 in 1 PAIL
9		0.36 g in 1 POUCH; Type 0: Not a Combination Product
10	NDC: 75213-001-10	12 in 1 CARTON	03/21/2020
10		150 in 1 PAIL
10		0.54 g in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/21/2020

Labeler - Hangzhou LUC Travel Products Co., LTD. (544043886)

Establishment
Name	Address	ID/FEI	Business Operations
Hangzhou LUC Travel Products Co., LTD.		544043886	manufacture(75213-001)