What is NDC 63083-9307?

63083-9307 is the product NDC for Uric Acid Combination 9307 (uric acid combination), Sodium carbonate 3 [hp_X]/29.5mL + 8 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?

Uric Acid Combination 9307 (Uric Acid Combination).

What is the active ingredient?

Sodium carbonate, Colchicum autumnale bulb, Strychnos nux-vomica seed, Toxicodendron pubescens leaf, Ferrosoferric phosphate, Lithium carbonate, Glutamine, 1,3-bis(Benzothiazol-2-ylthiomethyl)urea, Uric acid.

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 Uric Acid Combination 9307?

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.

Uric Acid Combination 9307 NDC 63083-9307

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-9307Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-9307Add 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
63083-9307-1	6308393070163083930701	29.5 mL in 1 BOTTLE, DROPPER (63083-9307-1)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): Uric Acid Combination 9307Suffix: 9307
Generic name (nonproprietary): uric acid combination
Active ingredients: Sodium carbonate — 3 [hp_X]/29.5mLColchicum autumnale bulb — 4 [hp_X]/29.5mLStrychnos nux-vomica seed — 6 [hp_X]/29.5mLToxicodendron pubescens leaf — 6 [hp_X]/29.5mLFerrosoferric phosphate — 8 [hp_X]/29.5mLLithium carbonate — 8 [hp_X]/29.5mLGlutamine — 12 [hp_X]/29.5mL1,3-bis(Benzothiazol-2-ylthiomethyl)urea — 12 [hp_X]/29.5mLUric acid — 12 [hp_X]/29.5mL
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: Allergens (Chemical structure)Amino Acids (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 63083-9307_f1791c2d-4b6a-4f62-9eec-defc383f3475SPL ID f1791c2d-4b6a-4f62-9eec-defc383f3475SPL set ID 3f136f86-a9ed-4a04-98cb-81abe33cd181UNII 45P3261C7T, 993QHL78E6, 269XH13919, 6IO182RP7A, 91GQH8I5F7, 2BMD2GNA4V, 0RH81L854J, 0214C2T14J, 268B43MJ25
Pharmacologic class: Amino Acid; Mood Stabilizer; 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

N463083930701 followed by a unit qualifier and the quantity

Package 63083-9307-01. 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 Jan 8, 2026.

Indications (excerpt from the label)

INDICATIONS For the temporary relief of minor joint pain or swelling, occasional headache, runny nose, skin irritation, or nausea.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63083-9307

What is NDC 63083-9307?: 63083-9307 is the product NDC for Uric Acid Combination 9307 (uric acid combination), Sodium carbonate 3 [hp_X]/29.5mL + 8 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?: Uric Acid Combination 9307 (Uric Acid Combination).
What is the active ingredient?: Sodium carbonate, Colchicum autumnale bulb, Strychnos nux-vomica seed, Toxicodendron pubescens leaf, Ferrosoferric phosphate, Lithium carbonate, Glutamine, 1,3-bis(Benzothiazol-2-ylthiomethyl)urea, Uric acid.
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 Uric Acid Combination 9307?: 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.

Uric Acid Combination 9307 (Uric acid combination) NDC 63083-9307