FDA.reportPublic FDA data

DRMITSUI HYDROCOLLOID WOUND - YIYANGYUAN LIFE SCIENCES (HONG KONG) CO., LIMITED

Manufacturer
YIYANGYUAN LIFE SCIENCES (HONG KONG) CO., LIMITED
Effective date
2026-06-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-06-16 05:10:28

Label at a glance#

ProductDRMITSUI HYDROCOLLOID WOUND
Active ingredientCARBOXYMETHYLCELLULOSE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Hydrocolloid

INACTIVE INGREDIENT SECTION

PRODUCT COMPOSITION: Outer layer substrate, Hydrocolloid, Protective layer.

OTC - PURPOSE SECTION

SOOTHING GEL

ACTIVATIONADVANCED MOISTURE CONTROL

PROTECTIVE & HYGIENIC BARRIER

HEALING-OPTIMIZED MICROCLIMATE

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

WARNINGS SECTION

Do not use if you have a known allergy to hydrocolloids.oDiscontinue use immediately if you experience any discomfort during use.This product is a daily-use item and is not intended to replace medications ormedical devices.

DOSAGE & ADMINISTRATION SECTION

This is a single-use product; use as soon as possible afteropening the package. Do not use if you have a known allergy to hydrocolloids.oDiscontinue use immediately if you experience any discomfort during use.This product is a daily-use item and is not intended to replace medications ormedical devices.

INDICATIONS & USAGE SECTION

Wash your hands thoroughly before and after treating the woundresidue before application. Ensure that the wound area is clean, dry, and freefrom any oily. Remove the release paper from the dressing. Maintain the adhesiveside of the dressing facing the wound. Accurately align the dressing, ensuringthe wound is situated at the centre. Apply dressing gently over the wound.oRemove the remaining clear release film (marked by arrows) from the dressing,and careful smooth it into place.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labelinglabeling

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87267-01287267-012-01

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
CARBOXYMETHYLCELLULOSE05JZI7B19XACTIB
PECTIN89NA02M4RXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
GELATIN2G86QN327LIACT
POLYURETHANE-62TBK645J3J8IACT

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
DRMITSUI HYDROCOLLOID WOUNDHYDROCOLLOIDYIYANGYUAN LIFE SCIENCES (HONG KONG) CO., LIMITED5438682c-6bc5-83f2-e063-6394a90ac3482026-06-14WarningsExact identifier
ndc (package): 87267-012-01
ndc (product): 87267-012
ndc11 (package): 87267001201
spl id: 5438682c-6bc6-83f2-e063-6394a90ac348
spl set id: 5438682c-6bc5-83f2-e063-6394a90ac348

Reported adverse events (FAERS/openFDA)#

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