WALGREENS ANTIBACTERIAL HAND WIPES- benzalkonium chloride cloth

Walgreens Antibacterial Hand Wipes by

Drug Labeling and Warnings

Walgreens Antibacterial Hand Wipes by is a Otc medication manufactured, distributed, or labeled by Walgreen Co.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzalkonium Chloride 0.11%

Purpose

Antibacterial

Uses

Decreases bacteria on skin

Warnings

For external use only

Do not use

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. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Adults and children 2 years and older: 

   Wipe hands thorough with product and allow to dry without wiping.

Children under 2 years of age: Consult a doctor before use.

Inactive ingredients

Water, Alcohol, Propylene Glycol, Phenoxyethanol, Lauryl Glucoside, Tetrasodium EDTA, 2-Bromo-2-Nitropropane-1,3-Diol, Citric Acid, Fragrance, Iodopropynyl Butylcarbamate, Aloe Barbadensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract.

SPL UNCLASSIFIED SECTION

Gentle cleansing

Kills 99.9% of germs

Hypoallergenic

DO NOT FLUSH

DISTRIBUTED BY: WALGREEN CO.

DEERFIELD, IL 60015

100% SATISFACTION GUARANTEED

walgreens.com  1-877-274-8358

©2024 Walgreen Co.  MADE IN CHINA

Packaging

INGREDIENTS AND APPEARANCE

WALGREENS ANTIBACTERIAL HAND WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-5189
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.11 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
EDETATE SODIUM (UNII: MP1J8420LU)
BRONOPOL (UNII: 6PU1E16C9W)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CHAMOMILE (UNII: FGL3685T2X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-5189-01	75 in 1 POUCH	05/21/2024
1		3.83 mL in 1 PATCH; Type 0: Not a Combination Product
2	NDC: 0363-5189-02	20 in 1 POUCH	05/21/2024
2		3.83 mL 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)	05/21/2024

Labeler - Walgreen Co. (008965063)