NDC codes

FDA NDC Directory
Product NDC (as listed)84984-002Labeler and product segments. Claims need a package NDC.
Product NDC at billing width84984-0002Add 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
84984-002-01849840002018498400020150 mg in 1 BOX (84984-002-01)Marketed from Apr 2, 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

Generic name (nonproprietary)
glycerin
Active ingredients
Laminaria japonica — .01 mg/50mgChamomile — .01 mg/50mgAvocado oil — .01 mg/50mgChondrus crispus carrageenan — .01 mg/50mg
Dosage form
Gel
Route
Topical
Labeler
Guangzhou Houkea Biotechnology Co., Ltd.NDC labeler code 84984
Product type
Over-the-counter drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Identifiers
Product ID 84984-002_44900a77-246a-bc1c-e063-6294a90a087bSPL ID 44900a77-246a-bc1c-e063-6294a90a087bSPL set ID 31c7490c-bcef-5e58-e063-6394a90ac8dbUNII WE98HW412B, FGL3685T2X, 6VNO72PFC1, UE856F2T78

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

N484984000201 followed by a unit qualifier and the quantity

Package 84984-0002-01. 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 84984-002

What is NDC 84984-002?
84984-002 is the product NDC for HOUKEA Rapid Mole Spot Elimination Gel, Laminaria japonica .01 mg/50mg + 3 more ingredients gel, listed with the FDA by Guangzhou Houkea Biotechnology Co., Ltd.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
HOUKEA Rapid Mole Spot Elimination Gel (Glycerin).
What is the active ingredient?
Laminaria japonica, Chamomile, Avocado oil, Chondrus crispus carrageenan.
Who is the labeler?
Guangzhou Houkea Biotechnology Co., Ltd., NDC labeler code 84984. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for HOUKEA Rapid Mole Spot Elimination Gel?
1 other product NDC are listed under this name. See all HOUKEA Rapid Mole Spot Elimination Gel NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other HOUKEA Rapid Mole Spot Elimination Gel NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
HOUKEA Rapid Mole Spot Elimination GelglycerinLaminaria japonica .01 mg/50mg + 3 more ingredientsGelTopicalGuangzhou Houkea Biotechnology Co., Ltd.84984-00684984-0006-01

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