BioPure Antibacterial Hand Wipes Fresh Scent

BioPure Antibacterial Hand Wipes Fresh Scent by

Drug Labeling and Warnings

BioPure Antibacterial Hand Wipes Fresh Scent 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 FRESH SCENT- benzalkonium chloride cloth 
QUEST USA CORP.

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BioPure Antibacterial Hand Wipes Fresh Scent

Drug Facts

Active ingredient

Benzalkonium Chloride 0.13%

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.
• Avoid freezing and excessive heat.

Inactive ingredients

Aloe Barbadensis Extract, Alpha-Tocopherol, Fragrance, Glycerin, Phenoxyethanol, Propylene Glycol, Purified Water

Questions?

call 718-975-2586

Package Labeling:

BIOPURE ANTIBACTERIAL HAND WIPES FRESH SCENT 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78691-015
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
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: 78691-015-00	75 in 1 CANISTER	09/30/2020	01/24/2023
1		4.13 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)	09/30/2020	01/24/2023

Labeler - QUEST USA CORP. (079869689)

Revised: 12/2023

Document Id: 0d6aa35f-9562-3f0e-e063-6394a90a1ad6

34390-5

Set id: b0b5174a-ce6f-c281-e053-2a95a90a33c5

Version: 3

Effective Time: 20231226