BioPure Antibacterial Hand Wipes

Manufacturer
Quest USA Corp
Effective date
2023-11-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:19:34

Label at a glance#

ProductBioPure Antibacterial Hand Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

Hand sanitizer to help reduce bacteria. For use when soap and water are not available.

Dosage and administration

Apply to hands, allow to dry without wiping. Children under 6 years of age should be supervised when using this product.

Storage and handling

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.12%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • Hand sanitizer to help reduce bacteria.
  • For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months old.
  • on open skin wounds.

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or rash appears and lasts.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply to hands, allow to dry without wiping.
  • Children under 6 years of age should be supervised when using this product.

​Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin, Phenoxyethanol, Propylene Glycol, Purified Water

Question?

OTC - QUESTIONS SECTION

call 718-975-2586

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78691-00378691-003-16

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
0d6adfc9-758d-b6df-e063-6294a90a1577ac8b22f4-57b3-10b9-e053-2995a90aaa482023-12-26WarningsExact identifier
spl set id: ac8b22f4-57b3-10b9-e053-2995a90aaa48

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.