HAND SANITIZING WIPES- benzalkonium chloride cloth

Hand Sanitizing Wipes by

Drug Labeling and Warnings

Hand Sanitizing Wipes by is a Otc medication manufactured, distributed, or labeled by Ez Products Of South Florida, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzalkonium Chloride (BZK) 0.1%

Purpose

Antibacterial

Use

• Decrease bacteria on the skin.

Warnings

For external use only.

When using this product

avoid contact with eyes.If contact occurs, rinse thoroughly with water.

Do not use

if irritation and redness develop.

Stop use and seek medical attention

if condition persists for more than 72 hours.

Keep out of reach of children.

If swallowed, seek medical attention or contact Poison Control Center.

DIRECTIONS

1. Locate tear-notch on the side of pouch. 2. Tear straight across to open.  3. Pull first wipe from center of roll and thread wipe through dispensing nozzle

Do not remove wipes roll from pouch.

Other information

• Dispose of wipe in the proper container.
• Do not flush down the toilet.

Inactive ingredients

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

Package Labeling:

INGREDIENTS AND APPEARANCE

HAND SANITIZING WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69446-220
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
BRONOPOL (UNII: 6PU1E16C9W)
ALCOHOL (UNII: 3K9958V90M)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CHAMOMILE (UNII: FGL3685T2X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
EDETATE SODIUM (UNII: MP1J8420LU)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69446-220-00	1500 in 1 BAG	04/30/2021
1		2.346 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 Drug	505G(a)(3)	04/30/2021

Labeler - Ez Products Of South Florida, LLC (113456060)