What is NDC 17312-437?

17312-437 is the product NDC for Natural Relief Arthritis Therapy, Apis mellifera 6 [hp_X]/1 + 6 more ingredients tablet, orally disintegrating, listed with the FDA by TRP Company. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Natural Relief Arthritis Therapy (Apis mellifera, Salicylic acid, Ruta graveolens, Toxicodendron pubescen, Lithium carbonate, Bryonia alba, Calcium fluoride).

What is the active ingredient?

Apis mellifera, Bryonia alba root, Calcium fluoride, Lithium carbonate, Toxicodendron pubescens leaf, Ruta graveolens flowering top, Salicylic acid.

TRP Company, NDC labeler code 17312. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Natural Relief Arthritis Therapy?

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.

Natural Relief Arthritis Therapy NDC 17312-437

NDC codes

FDA NDC Directory

Product NDC (as listed)17312-437Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17312-0437Add 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
17312-437-14	1731204371417312043714	1 BOTTLE in 1 PACKAGE (17312-437-14) / 70 TABLET, ORALLY DISINTEGRATING in 1 BOTTLEMarketed from Apr 30, 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): Natural Relief Arthritis Therapy
Generic name (nonproprietary): apis mellifera, salicylic acid, ruta graveolens, toxicodendron pubescen, lithium carbonate, bryonia alba, calcium fluoride
Active ingredients: Apis mellifera — 6 [hp_X]/1Bryonia alba root — 6 [hp_X]/1Calcium fluoride — 10 [hp_X]/1Lithium carbonate — 6 [hp_X]/1Toxicodendron pubescens leaf — 6 [hp_X]/1Ruta graveolens flowering top — 6 [hp_X]/1Salicylic acid — 3 [hp_X]/1
Dosage form: Tablet, Orally disintegrating
Route: Oral
Labeler: TRP CompanyNDC labeler code 17312
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 30, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 17312-437_436f7b11-402d-70e2-e063-6394a90a396fSPL ID 436f7b11-402d-70e2-e063-6394a90a396fSPL set ID 436f7af7-859e-f7af-e063-6294a90af508UNII 7S82P3R43Z, T7J046YI2B, O3B55K4YKI, 2BMD2GNA4V, 6IO182RP7A, N94C2U587S, O414PZ4LPZ
Pharmacologic class: Mood Stabilizer; Standardized Insect Venom 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

N417312043714 followed by a unit qualifier and the quantity

Package 17312-0437-14. 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 Nov 12, 2025.

Indications (excerpt from the label)

Uses* According to homeopathic indications these ingredients provide temporary relief from symptoms such as: Joint Pain Stiffness Swelling Immobility. *These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 17312-437

What is NDC 17312-437?: 17312-437 is the product NDC for Natural Relief Arthritis Therapy, Apis mellifera 6 [hp_X]/1 + 6 more ingredients tablet, orally disintegrating, listed with the FDA by TRP Company. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Natural Relief Arthritis Therapy (Apis mellifera, Salicylic acid, Ruta graveolens, Toxicodendron pubescen, Lithium carbonate, Bryonia alba, Calcium fluoride).
What is the active ingredient?: Apis mellifera, Bryonia alba root, Calcium fluoride, Lithium carbonate, Toxicodendron pubescens leaf, Ruta graveolens flowering top, Salicylic acid.
Who is the labeler?: TRP Company, NDC labeler code 17312. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Natural Relief Arthritis Therapy?: 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.