BIOPURE ANTIBACTERIAL HAND WIPES BENZALKONIUM CHLORIDE 0.12% - 250 WIPES- benzalkonium chloride cloth

BioPure Antibacterial Hand Wipes Benzalkonium Chloride 0.12% - 250 Wipes by

Drug Labeling and Warnings

BioPure Antibacterial Hand Wipes Benzalkonium Chloride 0.12% - 250 Wipes by is a Otc medication manufactured, distributed, or labeled by QUEST USA CORP.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzalkonium Chloride 0.12%

Purpose

Antibacterial

Uses

Hand sanitizer to help reduce bacteria. For use when soap and water are not available.

Warnings

For external use only.

Do not use

in children less than 2 months old. on open skin wounds.

When using this product

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if

irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

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

Directions

Apply to hands, allow to air dry without wiping. Children under 6 years of age should be supervised when using this product.

Other information

Store in a cool, dry place, between 15°-30° (59°-86°F). Avoid freezing and excessive heat above 40°C (104°F).

Inactive ingredients

Glycerin, Phenoxyethanol, Propylene Glycol, Purified Water

Questions?

call 718-975-2586

Package Labeling:

INGREDIENTS AND APPEARANCE

BIOPURE ANTIBACTERIAL HAND WIPES BENZALKONIUM CHLORIDE 0.12% - 250 WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78691-009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.2 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78691-009-00	250 in 1 CONTAINER	09/20/2020
1		2.8 mL 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)	09/20/2020

Labeler - QUEST USA CORP. (079869689)