ANTIBACTERIAL WET WIPES- benzalkonium chloride swab

Antibacterial Wet Wipes by

Drug Labeling and Warnings

Antibacterial Wet Wipes by is a Otc medication manufactured, distributed, or labeled by Hangzhou Zhongbo Industrial Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient
Benzalkonium chloride 0.115 percent

PURPOSE

Purpose: Antibacterial

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children, except with adult supervision.

WARNINGS

Warnings

For external use only
Keep out of the eyes. In case of eye contact, rinse with water.
If irritation develps discontinue use and consult a doctor if irritation persists more than 72 hours.
If swallowed, seek medical attention or contact a Poison Control Center.

INDICATIONS & USAGE

Uses

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

DOSAGE & ADMINISTRATION

Direction for use:

Thoroughly wipe hands and face as desired.
Allow to dry without wiping.
Discard wipe in trash receptacle after use. Do not flush.

INACTIVE INGREDIENT

Inactive Ingredients

Propylene glycol, 4Na EDTA, Sorbitol, Aloe Extract, Purified Water, Fragrance, Tocopherol Acetate (Vitamin E).

PRINCIPAL DISPLAY PANEL

Convenient Easy to use and carry anytime!

Clean-Up Use to wash up quickly when soap and water are not available2.2ex0em2.2ex0emMoisturize soothes and softens dry skin.

Antibacterial Wet Wipes contain soothing Aloe to help moisturize your skin and leave it feeling soft and smooth. Our Wet Wipes are thick and strong to help even the roughest skin.

Distributed by:
Greenbrier International, Inc.
Chesapeake, VA 23320
Made in China

Antibacterial Wet Wipes
Hands and Face Moisturizing Towelettes
with Aloe

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL WET WIPES 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 44992-6144
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.115 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
EDETIC ACID (UNII: 9G34HU7RV0)
SORBITOL (UNII: 506T60A25R)
ALOE (UNII: V5VD430YW9)
WATER (UNII: 059QF0KO0R)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44992-6144-4	20 in 1 PACKAGE	12/06/2010	07/30/2020
1	NDC: 44992-6144-3	100 mg in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 44992-6144-2	3 in 1 PACKAGE	12/06/2010	07/30/2020
2	NDC: 44992-6144-1	1000 mg in 1 PACKET; 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	part333E	12/06/2010	07/30/2020

Labeler - Hangzhou Zhongbo Industrial Co., Ltd. (421265530)

Establishment
Name	Address	ID/FEI	Business Operations
Hangzhou Zhongbo Industrial Co., Ltd.		421265530	manufacture(44992-6144)