WET WIPES ANTIBACTERIAL TRAVEL

WET WIPES ANTIBACTERIAL TRAVEL by

Drug Labeling and Warnings

WET WIPES ANTIBACTERIAL TRAVEL by is a Otc medication manufactured, distributed, or labeled by International Wholesale, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

WET WIPES ANTIBACTERIAL TRAVEL- benzalkonium chloride cloth 
International Wholesale, Inc.

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WET WIPES ANTIBACTERIAL TRAVEL

Drug Facts

Active Ingredient (by volume)

Benzalkonium Chloride 0.1%

Purpose

Antibacterial

Uses

• decreases bacteria on skin.

WARNINGS

For external use only

Do not use:

Over large areas of the body if you are allergic to any of the ingredients.

When using this product

do not get into eyes. If contact occurs, rinse thoroughly with water.

Stop use and ask a doctor if 

irritation or rash develops and continues for more than 72 hours.

Keep out of reach of children.

For children under 2 years ask a doctor before use. For children use under adult supervision.

Directions

Do not expose to direct sunlight, preferably place them in a cool place. Do not use on furniture. Do not flush down toilets, dispose in trash recepticals.

Remove lid and open the seal. Pull up the corner of the center sheet, twist it and thread through the dispenser split in the lid. Pull sheet out at an angle. When finished close lid flap to retain moisture.

Inactive Ingredients:

Water, Propylene Glycol, Cocamidopropyl Betaine, PEG-7 Glyceryl Cocoate, Fragrance, Benzyl Alcohol, Methylchloroisothiazolinone, Methylisothiazolinone, Tetrasodium EDTA, PEG-40 Hydrogenated Castor Oil, Cetrimonium Chloride, Citric Acid, Aloe Vera Extract, Alphatocopherol, Acetate (Vitamin E)

Package Labeling:

WET WIPES ANTIBACTERIAL TRAVEL 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52862-650
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)
BENZYL ALCOHOL (UNII: LKG8494WBH)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
EDETATE SODIUM (UNII: MP1J8420LU)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
ACETATE ION (UNII: 569DQM74SC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52862-650-00	30 in 1 POUCH	09/01/2022	12/31/2023
1		3.63 g in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	09/01/2022	12/31/2023

Labeler - International Wholesale, Inc. (161872676)

Revised: 12/2023

Document Id: 0da85c6d-4e33-ef90-e063-6294a90a011d

34390-5

Set id: 114f16cf-81a8-4b93-9e4c-d1cad09760b3

Version: 6

Effective Time: 20231229