BioPure Antibacterial Hand Wipes Unscented

BioPure Antibacterial Hand Wipes Unscented by

Drug Labeling and Warnings

BioPure Antibacterial Hand Wipes Unscented 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 UNSCENTED- benzalkonium chloride cloth 
QUEST USA CORP.

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BioPure Antibacterial Hand Wipes Unscented

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. Avoid freezing and excessive heat.

Inactive ingredients

Glycerin, Methylchloroisothiazolinone, Phenoxyethanol, Propylene Glycol, Purified Water

Question?

call 718-975-2586

Package Labeling:

BIOPURE ANTIBACTERIAL HAND WIPES UNSCENTED 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78691-008
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)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78691-008-00	1400 in 1 BAG	09/20/2020	12/31/2023
1		2.29 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	12/31/2023

Labeler - QUEST USA CORP. (079869689)

Revised: 12/2023

Document Id: 0d6abff2-552b-32c5-e063-6394a90aad70

34390-5

Set id: ae2fdb32-05c3-6d16-e053-2995a90a552d

Version: 3

Effective Time: 20231226