What is NDC 85631-003?

85631-003 is the product NDC for Gout Relief 3310-S, Glucosamine hydrochloride 130 mg/1.3g + 9 more ingredients capsule, 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 3310-S (Celery seed, Medicago sativa whole,Chicory root).

What is the active ingredient?

Glucosamine hydrochloride, Morus alba leaf, Licorice, Puerarin, Buckwheat, Sodium chloride, Medicago sativa whole, Tea leaf, Celery seed, Chicory root.

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 3310-S?

2 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Gout Relief 3310-S NDC 85631-003 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)85631-003Labeler and product segments. Claims need a package NDC.

Product NDC at billing width85631-0003Add 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
85631-003-01	85631000301	60 CAPSULE in 1 BOX (85631-003-01) / 1.3 g in 1 CAPSULEMarketed from Jul 28, 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 3310-S
Generic name (nonproprietary): celery seed, medicago sativa whole,chicory root
Active ingredients: Glucosamine hydrochloride — 130 mg/1.3gMorus alba leaf — 39 mg/1.3gLicorice — 2.6 mg/1.3gPuerarin — 65 mg/1.3gBuckwheat — 91 mg/1.3gSodium chloride — 26 mg/1.3gMedicago sativa whole — 260 mg/1.3gTea leaf — 65 mg/1.3gCelery seed — 260 mg/1.3gChicory root — 234 mg/1.3g
Dosage form: Capsule
Route: Oral
Labeler: Bispit Canada Ltd.NDC labeler code 85631
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 28, 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)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Plant Proteins (Chemical structure)
Identifiers: Product ID 85631-003_3b610399-6dbe-c84f-e063-6394a90afd5eSPL ID 3b610399-6dbe-c84f-e063-6394a90afd5eSPL set ID 3afaa7d9-3de3-52d9-e063-6294a90a54ecUNII 750W5330FY, M8YIA49Q2P, 61ZBX54883, Z9W8997416, N0Y68724R3, 451W47IQ8X, DJO934BRBD, GH42T47V24, 1G1EAA320L, 090CTY533NUPC 0850066597200
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Osmotic Laxative

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

N485631000301 followed by a unit qualifier and the quantity

Package 85631-0003-01. 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 Aug 2, 2025.

Indications (excerpt from the label)

Dissolved CrystallizationKidney StoneGallstone< Urinary Calculus

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 85631-003

What is NDC 85631-003?: 85631-003 is the product NDC for Gout Relief 3310-S, Glucosamine hydrochloride 130 mg/1.3g + 9 more ingredients capsule, 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 3310-S (Celery seed, Medicago sativa whole,Chicory root).
What is the active ingredient?: Glucosamine hydrochloride, Morus alba leaf, Licorice, Puerarin, Buckwheat, Sodium chloride, Medicago sativa whole, Tea leaf, Celery seed, Chicory root.
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 3310-S?: 2 other product NDCs are listed under this name. See all Gout Relief 3310-S 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 Gout Relief 3310-S NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Gout Relief 3310-Smedicago sativa whole chicory root	Coix lacryma-jobi seed 104 mg/1.3g + 8 more ingredients	CapsuleOral	Bispit Canada Ltd.	85631-006	85631-0006-01
Gout Relief 3310-Scelery seed medicago sativa whole	Lysimachia christinae whole 65 mg/1.3g + 9 more ingredients	CapsuleOral	Bispit Canada Ltd.	85631-001	85631-0001-01