FDA.reportPublic FDA data

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#

ProductAntibacterial Hand Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

●Apply to hands, allow to air 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, 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

Benzalkonium Chloride 0.13%

OTC - PURPOSE SECTION

Antimicroblal

USE

DOSAGE & ADMINISTRATION SECTION

●Hand sanitizer to help reduce bacteria

●For use when soap and water are not available.

OTC - DO NOT USE SECTION

●in children less than 2 months old.

●on open skin wounds

WARNINGS SECTION

For external use only.

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

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition

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.

INACTIVE INGREDIENT SECTION

Purified water

Glycerin

Phenoxyethanol

Propylene Glycol

Aleo Barbadensis Extract

Alpha-Tocopherol

Fragrance

DIRECTIONS

INDICATIONS & USAGE SECTION

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

●Children under 6 years of age should be supervised when using this product

THER 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）

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78691-10078691-100-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
JASMINUM OFFICINALE FLOWER0Q8K841432IACT
PHENOXYETHANOLHIE492ZZ3TIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT
ALOE VERA WHOLEKIZ4X2EHYXIACT
ALPHA-TOCOPHEROLH4N855PNZ1IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
0f3056ee-3f47-a582-e063-6294a90abb06d4cfde29-2120-2c7f-e053-2995a90ac8252024-01-17WarningsExact identifier
spl id: 0f3056ee-3f47-a582-e063-6294a90abb06
spl set id: d4cfde29-2120-2c7f-e053-2995a90ac825

Reported adverse events (FAERS/openFDA)#

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