Gout Symptom Relief NDC 57955-9975

NDC codes

FDA NDC Directory

Product NDC (as listed)57955-9975Labeler and product segments. Claims need a package NDC.

Product NDC at billing width57955-9975Add 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
57955-9975-2	57955997502	59 mL in 1 BOTTLE, SPRAY (57955-9975-2)Marketed from Mar 10, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 Symptom Relief
Generic name (nonproprietary): ammon phos, belladonna, colchicum autumnale, formicum acidum, fraxinus excelsior, ledum palustre, natrum carbonicum, nux vomica and urtica urens.
Active ingredients: Ammonium phosphate, Dibasic — 10 [hp_X]/59mLAtropa belladonna — 10 [hp_X]/59mLColchicum autumnale bulb — 10 [hp_X]/59mLFormic acid — 10 [hp_X]/59mLFraxinus excelsior bark — 10 [hp_X]/59mLFraxinus excelsior leaf — 10 [hp_X]/59mLRhododendron tomentosum leafy twig — 10 [hp_X]/59mLSodium carbonate — 10 [hp_X]/59mLStrychnos nux-vomica seed — 10 [hp_X]/59mLUrtica urens whole — 10 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: King Bio Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 10, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 57955-9975_4590e343-960e-4fa7-888e-8b9ed5ad93bdSPL ID 4590e343-960e-4fa7-888e-8b9ed5ad93bdSPL set ID 41dc03fc-169b-4691-bd62-9a41d7a6d2f7UNII 10LGE70FSU, WQZ3G9PF0H, 993QHL78E6, 0YIW783RG1, R6KCX5H8I2, RC38362Q7M, 877L01IZ0P, 45P3261C7T, 269XH13919, IHN2NQ5OF9
Pharmacologic class: 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

N457955997502 followed by a unit qualifier and the quantity

Package 57955-9975-02. 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 Mar 6, 2026.

Indications (excerpt from the label)

Uses † temporary relief of symptoms in toes, heels, feet, or joints: discomforts cramping tender or itchy joints † Claims based on traditional Homeopathic practice, not accepted medical evidence, not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)