DUCO

Manufacturer
BIOCHEM KOREA CO., LTD
Effective date
2021-01-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:37:32

Label at a glance#

ProductDUCO
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE 0.1%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

PERFUME 0.1%

WATER 99.8%

KEEP OUT OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF CHILDREN.

WARNING

WARNINGS SECTION

External use only

When using this product, do not use it in or near the eyes. In case of contact, rinse eyes thoroughly with water.

ASK DOCTOR

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if irritation or rash occurs.

If swallowed, get medical help or contact poison control center right away.

DO NOT USE

OTC - DO NOT USE SECTION

When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water

Stop use if irritation or rash occurs.

DIRECTION

DOSAGE & ADMINISTRATION SECTION

Thoroughly wipe hands with the wipe.

Discard properly. Not flushable.

Be sure to close the lid to keep wipes moist.

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Use hand sanitizer to help reduce bacteria on the skin that could cause disease. Recommended for repeated use.

PURPOSE

OTC - PURPOSE SECTION

Antiseptic hand-cleaning to reduce germs on hands.

PACKAGE LABEL AND PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DUCO 80 Disinfecting WipesDUCO 80 Disinfecting Wipes

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74085-0012-12022-07-29C16284748780-1e4f33bdf-ae3d-d8a0-e053-dadaa90a6e4eb9e80933-3434-d471-e053-2995a90a84e4
74085-0012-22022-07-29C16284748780-1e4f33bdf-ae3d-d8a0-e053-dadaa90a6e4eb9e80933-3434-d471-e053-2995a90a84e4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74085-0012-1DUCO260 g in 1 CANISTERLIQUID2601
74085-0012-2DUCO750 g in 1 CANISTERLIQUID7501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74085-0012DUCO (DUCO DISINFECTING WIPES) LIQUID [BIOCHEM KOREA CO., LTD]1Legacy NDC, 2 package rows20210129_b9e80933-3434-d471-e053-2995a90a84e4.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74085-001274085-0012-1, 74085-0012-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT

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
b9e80933-3435-d471-e053-2995a90a84e4b9e80933-3434-d471-e053-2995a90a84e42021-01-27WarningsExact identifier
spl id: b9e80933-3435-d471-e053-2995a90a84e4
spl set id: b9e80933-3434-d471-e053-2995a90a84e4

Reported adverse events (FAERS/openFDA)#

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