BioPure Antibacterial Hand Wipes

BioPure Antibacterial Hand Wipes by

Drug Labeling and Warnings

BioPure Antibacterial Hand Wipes by is a Otc medication manufactured, distributed, or labeled by Quest USA Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BIOPURE ANTIBACTERIAL HAND WIPES- benzalkonium chloride cloth 
Quest USA Corp

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BioPure Antibacterial Hand Wipes

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.12%

Purpose

Antimicrobial

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

do not get in eyes.  If contact is made rinse thoroughly with water.

Stop use and ask a doctor if

irritation or rash appears and lasts.

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 dry without wiping.
• Children under 6 years of age should be supervised when using this product.

​Other information

• Store in a cool, dry place.
• Avoid freezing and excessive heat.

Inactive ingredients

Glycerin, Phenoxyethanol, Propylene Glycol, Purified Water

Question?

call 718-975-2586

Package Labeling:

BIOPURE ANTIBACTERIAL HAND WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78691-003
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
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78691-003-16	1600 in 1 BAG	09/15/2020	08/28/2022
1		3.44 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)	09/15/2020	08/28/2022

Labeler - Quest USA Corp (079869689)

Revised: 12/2023

Document Id: 0d6adfc9-758d-b6df-e063-6294a90a1577

34390-5

Set id: ac8b22f4-57b3-10b9-e053-2995a90aaa48

Version: 4

Effective Time: 20231226