BIOPURE ANTIBACTERIAL HAND WIPE BERRY STRAWBERRY- benzalkonium chloride cloth

Biopure Antibacterial Hand Wipe Berry Strawberry by

Drug Labeling and Warnings

Biopure Antibacterial Hand Wipe Berry Strawberry 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 0.13%

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 ues

• on 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 Leaf Extract, Alpha-Tocopherol, Fragrance, Glycerin, Phenoxyethanol, Propylene Glycol, Water

Questions?

call 718-975-2586

Anti-Bacterial Hand Wipe-Berry Strawberry

INGREDIENTS AND APPEARANCE

BIOPURE ANTIBACTERIAL HAND WIPE BERRY STRAWBERRY 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78691-035
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
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.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: 78691-035-00	50 mL in 1 CANISTER; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)	01/09/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	01/09/2026

Labeler - Quest USA Corp (079869689)

Registrant - Quest USA Corp (079869689)