FDA.reportPublic FDA data

Biopure Sanitizing Alcohol Free Wipes

Manufacturer
QUEST USA CORP | Zhangzhou Zhongnan Nursing Products Co.,Ltd.
Effective date
2020-06-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:25:43

Label at a glance#

ProductBiopure Sanitizing Alcohol Free Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Indications and uses

Hand Sanitizer to help reduce bacteria on the skin

Dosage and administration

Wet hands thoroughly with product and allow to dry. Children under 6 years of age should be supervised when using BIOPURE products.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.12%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only. Flammable. keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

  • In children less than 2 months of age
  • On open skin wounds

When using this product

OTC - WHEN USING SECTION

When using this product do not get in eyes. If contact is made rinse thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and allow to dry.
  • Children under 6 years of age should be supervised when using BIOPURE products.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Decyl Glucoside, Phenoxyethanol, Glycerin, Fragrance (Parfum)

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1600 Wipes; NDC - 78691-697-16

Biopure Sanitizing Alcohol Free WipesBiopure Sanitizing Alcohol Free Wipes

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78691-697-162022-12-28C16284748780-1c7ccaba7-1ef3-fd44-e053-dadaa90aa01ba7ab3f85-143d-bc41-e053-2a95a90a42c0
78691-697-162021-07-23C16284748780-1c7ccaba7-1ef3-fd44-e053-dadaa90aa01ba7ab3f85-143d-bc41-e053-2a95a90a42c0

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78691-69778691-697-16

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
PHENOXYETHANOLHIE492ZZ3TIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
DECYL GLUCOSIDEZ17H97EA6YIACT
GLYCERINPDC6A3C0OXIACT

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
f0e5874f-6458-05ac-e053-2a95a90a2b04a7ab3f85-143d-bc41-e053-2a95a90a42c02022-12-28WarningsExact identifier
spl set id: a7ab3f85-143d-bc41-e053-2a95a90a42c0

Reported adverse events (FAERS/openFDA)#

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