OSEQUE SAFETY HAND WET WIPES

Manufacturer
SONGHAK CO., LTD. | NAICO
Effective date
2020-07-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:20:25

Label at a glance#

ProductOSEQUE SAFETY HAND WET WIPES
Active ingredientBenzalkonium Chloride
Label structure9 sections

Indications and uses

■ hand sanitizing wipes to help reduce bacteria on the skin. For use when soap and water not available

Dosage and administration

■ thoroughly wipes hands with cloth ■ rub hands together until dry

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Glycerin, Sodium Benzoate, Polysorbate 20, Ethylhexylglycerin,, Disodium EDTA, Citric Acid, Tocopheryl Acetate, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Fragrance

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

WARNINGS

WARNINGS SECTION

For external use only
--------------------------------------------------------------------------------------------------------
Do not use
■ on infants
■ on open skin wounds
--------------------------------------------------------------------------------------------------------
When using this product
■ avoid getting into the eyes
■ In case of eye contact immediately flush eyes thoroughly with water
--------------------------------------------------------------------------------------------------------
Stop use and ask a doctor
■ if irritation or redness develops
■ conditions persist for more than 72 hours
■ redness is present

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

■ in case of accidental ingestion, contact a doctor or Poison Center immediately

Uses

INDICATIONS & USAGE SECTION

■ hand sanitizing wipes to help reduce bacteria on the skin. For use when soap and water not available

Directions

DOSAGE & ADMINISTRATION SECTION

■ thoroughly wipes hands with cloth
■ rub hands together until dry

Other information

OTHER SAFETY INFORMATION

■ Storage in a cool, dry place, Avoid freezing and excessive heat above 40 ℃ (104 ℉)
■ Do not flush

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of packetImage of packet

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59370-150-012024-12-19C16284748780-1d6a99b39-7784-a426-e053-dadaa90af4c283066bb9-d3b3-4b03-bb3d-2cbf13e8a208
59370-150-012022-01-28C16284748780-1d6a99b39-7784-a426-e053-dadaa90af4c283066bb9-d3b3-4b03-bb3d-2cbf13e8a208

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59370-15059370-150-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
28fa4b17-b857-fdce-e063-6294a90a5b2583066bb9-d3b3-4b03-bb3d-2cbf13e8a2082024-12-11WarningsExact identifier
spl set id: 83066bb9-d3b3-4b03-bb3d-2cbf13e8a208

Reported adverse events (FAERS/openFDA)#

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