BIOPURE ANTIBACTERIAL HAND WIPES BENZALKONIUM CHLORIDE 0.12% - 250 WIPES- benzalkonium chloride cloth 
QUEST USA CORP.

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BioPure Antibacterial Hand Wipes Benzalkonium Chloride 0.12% - 250 Wipes

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:

Label2

BIOPURE ANTIBACTERIAL HAND WIPES BENZALKONIUM CHLORIDE 0.12% - 250 WIPES 
benzalkonium chloride cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78691-009
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.2 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:78691-009-00250 in 1 CONTAINER09/20/2020
12.8 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)09/20/2020
Labeler - QUEST USA CORP. (079869689)

Revised: 12/2023
Document Id: 0d964c7c-4d8b-e478-e063-6294a90a4f2e
Set id: ae2fdb32-05c6-6d16-e053-2995a90a552d
Version: 3
Effective Time: 20231228
 
QUEST USA CORP.