ANTIBACTERIAL WET- benzalkonium chloride liquid

Antibacterial Wet by

Drug Labeling and Warnings

Antibacterial Wet by is a Otc medication manufactured, distributed, or labeled by Xi'an Livingbond Nonwoven Products Corp., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Antibacterial

Uses:

For hand washing to decrease bacteria on the skin. May be used on face, arms and legs.

Warnings:

For external use only.

Keep out of reach of children,

except with adult supervision. Keep out of eyes. In case of contact, rinse with water. If irritation or rash develops, discontinue use. Consult doctor if irritation persists for more than 72 hours. If swallowed, seek medical attention or contact a Poison Control Center.

Directions:

Tear open. Unfold the wipe. Clean hands or affected area and discard.

Inactive Ingredients:

Water, Glycerin, Lauryl Glucoside, DMDM, Hydantoin, Aloe Barbadensis Leaf Extract, Disodium EDTA, PEG 12, Dimethicone, Panthenol,  Chamomila Recutita (Matricaria) Extract, Lodopropynyl Butlycarbamae, Tocopheryl Acetate (Vitamin E), Allantoin.

Package Labeling:

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL WET 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50014-110
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
HYDANTOIN (UNII: I6208298TA)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
POLYETHYLENE GLYCOL 12000 (UNII: VM53EE110J)
DIMETHICONE (UNII: 92RU3N3Y1O)
PANTHENOL (UNII: WV9CM0O67Z)
MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
ALLANTOIN (UNII: 344S277G0Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50014-110-01	1 in 1 BAG	11/27/2017
1		0.1 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
2	NDC: 50014-110-30	30 in 1 BAG	11/27/2017
2		0.1 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
3	NDC: 50014-110-50	50 in 1 CANISTER	11/27/2017
3		0.1 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	11/27/2017

Labeler - Xi'an Livingbond Nonwoven Products Corp., Ltd. (529686742)

Establishment
Name	Address	ID/FEI	Business Operations
Xi'an Livingbond Nonwoven Products Corp., Ltd.		529686742	manufacture(50014-110)