BIOPURE 50CT ANTIBACTERIAL HAND WIPES

Manufacturer
Quest USA Corp. | Osike Cosmetics Co., Ltd.
Effective date
2024-01-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:14:07

Label at a glance#

ProductBIOPURE 50CT ANTIBACTERIAL HAND WIPES
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

●Hand sanitizer to help reduce bacteria that potentially cause disease. ●For use when soap and water are not available.

Dosage and administration

●Apply to hands, allow to air dry without wiping. ●Discard wipe in trash receptacle after use. ● Do not flush.

Storage and handling

●Store in a cool, dry place, between 15°C-30°C(59°F-86°F) ●Avoid freezing and excessive heat above 40°C(104°F)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

OTC - PURPOSE SECTION

Antiseptic

Uses

DOSAGE & ADMINISTRATION SECTION

●Hand sanitizer to help reduce bacteria that potentially cause disease.

●For use when soap and water are not available.

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame.

OTC - DO NOT USE SECTION

●in children less than 2 months of age.

●on open skin wounds

OTC - WHEN USING SECTION

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

INDICATIONS & USAGE SECTION

●Apply to hands, allow to air dry without wiping.

●Discard wipe in trash receptacle after use.

● Do not flush.

Other information

STORAGE AND HANDLING SECTION

●Store in a cool, dry place, between 15°C-30°C(59°F-86°F)

●Avoid freezing and excessive heat above 40°C(104°F)

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Extract, Alpha-Tocopherol, Glycerin, Purified Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78691-20078691-200-01

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
0f3069cb-d734-ae08-e063-6294a90a3f0cd56f8533-e139-048a-e053-2995a90afa202024-01-17WarningsExact identifier
spl id: 0f3069cb-d734-ae08-e063-6294a90a3f0c
spl set id: d56f8533-e139-048a-e053-2995a90afa20

Reported adverse events (FAERS/openFDA)#

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