What is NDC 85631-009?

85631-009 is the product NDC for Gout Relief 3310A Plus, Licorice 1 mg/g + 9 more ingredients tablet, listed with the FDA by Bispit Canada Ltd.. It has 1 package NDC, shown above in 10- and 11-digit form.

What is the active ingredient?

Licorice, Medicago sativa whole, Buckwheat, Fu ling, Chicory root, Morus alba leaf, Anserine, Tea leaf, Coix lacryma-jobi seed, Glucosamine hydrochloride.

Bispit Canada Ltd., NDC labeler code 85631. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Gout Relief 3310A Plus?

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.

Gout Relief 3310A Plus NDC 85631-009 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)85631-009Labeler and product segments. Claims need a package NDC.

Product NDC at billing width85631-0009Add 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 NDC	11-digit (billing)	Package	Copy
85631-009-01	85631000901	60 CAPSULE in 1 BOX (85631-009-01) / 1 g in 1 CAPSULEMarketed from Sep 5, 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): Gout Relief 3310A Plus
Generic name (nonproprietary): gout relief 3310a plus
Active ingredients: Licorice — 1 mg/gMedicago sativa whole — 150 mg/gBuckwheat — 40 mg/gFu ling — 10 mg/gChicory root — 180 mg/gMorus alba leaf — 75 mg/gAnserine — 350 mg/gTea leaf — 34 mg/gCoix lacryma-jobi seed — 40 mg/gGlucosamine hydrochloride — 70 mg/g
Dosage form: Tablet
Route: Oral
Labeler: Bispit Canada Ltd.NDC labeler code 85631
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 5, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Dietary Proteins (Chemical structure)Grain Proteins (EXT)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers: Product ID 85631-009_3e1d060f-1584-3b66-e063-6394a90a5996SPL ID 3e1d060f-1584-3b66-e063-6394a90a5996SPL set ID 3e0a4e26-61b6-01cb-e063-6294a90a4efcUNII 61ZBX54883, DJO934BRBD, N0Y68724R3, XH37TWY5O4, 090CTY533N, M8YIA49Q2P, HDQ4N37UGV, GH42T47V24, 4Q4V6NTZ1F, 750W5330FYUPC 0850066597217
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract

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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N485631000901 followed by a unit qualifier and the quantity

Package 85631-0009-01. 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 Sep 6, 2025.

Indications (excerpt from the label)

Applicable Population:patient with gout,high uric acid, depositionof urate crystal, kidney stone and bladder stone.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 85631-009

What is NDC 85631-009?: 85631-009 is the product NDC for Gout Relief 3310A Plus, Licorice 1 mg/g + 9 more ingredients tablet, listed with the FDA by Bispit Canada Ltd.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Gout Relief 3310A Plus.
What is the active ingredient?: Licorice, Medicago sativa whole, Buckwheat, Fu ling, Chicory root, Morus alba leaf, Anserine, Tea leaf, Coix lacryma-jobi seed, Glucosamine hydrochloride.
Who is the labeler?: Bispit Canada Ltd., NDC labeler code 85631. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Gout Relief 3310A Plus?: 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.