What is NDC 63083-2080?

63083-2080 is the product NDC for Gout Drops 2080 (gout drops), Bryonia alba root 4 [hp_X]/59mL + 9 more ingredients liquid, listed with the FDA by Professional Complementary Health Formulas. It has 1 package NDC, shown above in 10- and 11-digit form.

What is the active ingredient?

Bryonia alba root, Solanum dulcamara whole, Rhododendron tomentosum leafy twig, Arnica montana whole, Benzoic acid, Colchicum autumnale bulb, Lithium carbonate, Urtica urens whole, Formica rufa, Lycopodium clavatum spore.

Professional Complementary Health Formulas, NDC labeler code 63083. 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 Drops 2080?

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 Drops 2080 NDC 63083-2080 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-2080Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-2080Add 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
63083-2080-2	6308320800263083208002	59 mL in 1 BOTTLE, DROPPER (63083-2080-2)Marketed from Aug 15, 1985

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 Drops 2080Suffix: 2080
Generic name (nonproprietary): gout drops
Active ingredients: Bryonia alba root — 4 [hp_X]/59mLSolanum dulcamara whole — 4 [hp_X]/59mLRhododendron tomentosum leafy twig — 4 [hp_X]/59mLArnica montana whole — 6 [hp_X]/59mLBenzoic acid — 6 [hp_X]/59mLColchicum autumnale bulb — 6 [hp_X]/59mLLithium carbonate — 6 [hp_X]/59mLUrtica urens whole — 6 [hp_X]/59mLFormica rufa — 12 [hp_X]/59mLLycopodium clavatum spore — 12 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: Professional Complementary Health FormulasNDC labeler code 63083
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 15, 1984
Listing expires: Dec 31, 2027
Other FDA classes: Ammonium Ion Binding Activity (Mechanism)
Identifiers: Product ID 63083-2080_de14e93f-43cf-4282-9aa8-58808df90c38SPL ID de14e93f-43cf-4282-9aa8-58808df90c38SPL set ID 30696295-01f6-4a50-a932-76fdc7c0501aUNII T7J046YI2B, G72JA9DHK5, 877L01IZ0P, O80TY208ZW, 8SKN0B0MIM, 993QHL78E6, 2BMD2GNA4V, IHN2NQ5OF9, 55H0W83JO5, C88X29Y479
Pharmacologic class: Mood Stabilizer; Nitrogen Binding Agent

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

N463083208002 followed by a unit qualifier and the quantity

Package 63083-2080-02. 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 Jan 8, 2026.

Indications (excerpt from the label)

INDICATIONS For the temporary relief of pain, inflammation, or stiffness of small joints.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63083-2080

What is NDC 63083-2080?: 63083-2080 is the product NDC for Gout Drops 2080 (gout drops), Bryonia alba root 4 [hp_X]/59mL + 9 more ingredients liquid, listed with the FDA by Professional Complementary Health Formulas. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Gout Drops 2080 (Gout Drops).
What is the active ingredient?: Bryonia alba root, Solanum dulcamara whole, Rhododendron tomentosum leafy twig, Arnica montana whole, Benzoic acid, Colchicum autumnale bulb, Lithium carbonate, Urtica urens whole, Formica rufa, Lycopodium clavatum spore.
Who is the labeler?: Professional Complementary Health Formulas, NDC labeler code 63083. 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 Drops 2080?: 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.

Gout Drops 2080 (Gout drops) NDC 63083-2080