NDC codes

FDA NDC Directory
Product NDC (as listed)87267-012Labeler and product segments. Claims need a package NDC.
Product NDC at billing width87267-0012Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
87267-012-018726700120115 PATCH in 1 BOX (87267-012-01) / 10 g in 1 PATCHMarketed from Jun 14, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Drmitsui Hydrocolloid Wound
Generic name (nonproprietary)
hydrocolloid
Active ingredients
Carboxymethylcellulose — 60 g/100g
Dosage form
Patch
Route
Topical
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication 505G(a)(3)
Marketing start
Listing expires
Identifiers
Product ID 87267-012_5438682c-6bc6-83f2-e063-6394a90ac348SPL ID 5438682c-6bc6-83f2-e063-6394a90ac348SPL set ID 5438682c-6bc5-83f2-e063-6394a90ac348UNII 05JZI7B19XUPC 4573638420626

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N487267001201 followed by a unit qualifier and the quantity

Package 87267-0012-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

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.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 87267-012

What is NDC 87267-012?
87267-012 is the product NDC for Drmitsui Hydrocolloid Wound (hydrocolloid), Carboxymethylcellulose 60 g/100g patch, listed with the FDA by YIYANGYUAN LIFE SCIENCES (HONG KONG) CO., LIMITED. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Drmitsui Hydrocolloid Wound (Hydrocolloid).
What is the active ingredient?
Carboxymethylcellulose.
Who is the labeler?
YIYANGYUAN LIFE SCIENCES (HONG KONG) CO., LIMITED, NDC labeler code 87267. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Drmitsui Hydrocolloid Wound?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under 505G(a)(3)

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

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Wet Wipes Antibacterial Hand Wipes, Travel Packbenzethonium chlorideBenzethonium chloride 1.3 mg/mLClothTopicalGlobal Import Sales LLC72146-037
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