NDC codes

FDA NDC Directory
Product NDC (as listed)84989-004Labeler and product segments. Claims need a package NDC.
Product NDC at billing width84989-0004Add 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
84989-004-01849890004018498900040120 mg in 1 BOX (84989-004-01)Marketed from Apr 24, 2025

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)
XIMONTH Wart Remover
Generic name (nonproprietary)
glycerin
Active ingredients
Artemisia vulgaris root — .004 mg/20mgApis mellifera venom — .004 mg/20mgHoney — .004 mg/20mg
Dosage form
Ointment
Route
Topical
Labeler
Shantou Ximonth Biotechnology Co., Ltd.NDC labeler code 84989
Product type
Over-the-counter drug
Marketing category
OTC monograph drugApplication M 014
Marketing start
Listing expires
Identifiers
Product ID 84989-004_448b7147-f044-c50a-e063-6294a90a2f75SPL ID 448b7147-f044-c50a-e063-6294a90a2f75SPL set ID 337d4d37-c2d6-44d3-e063-6294a90a77ceUNII 32MP823R8S, 76013O881M, Y9H1V576FH

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

N484989000401 followed by a unit qualifier and the quantity

Package 84989-0004-01. 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 .

Full label on DailyMed (opens in a new tab)

About NDC 84989-004

What is NDC 84989-004?
84989-004 is the product NDC for XIMONTH Wart Remover (glycerin), Artemisia vulgaris root .004 mg/20mg + 2 more ingredients ointment, listed with the FDA by Shantou Ximonth Biotechnology Co., Ltd.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
XIMONTH Wart Remover (Glycerin).
What is the active ingredient?
Artemisia vulgaris root, Apis mellifera venom, Honey.
Who is the labeler?
Shantou Ximonth Biotechnology Co., Ltd., NDC labeler code 84989. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for XIMONTH Wart Remover?
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 M 014

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

FDA NDC Directory listings under M 014
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