Thio Combination 9306 (thio combination) NDC 63083-9306

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-9306Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-9306Add 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
63083-9306-1	63083930601	29.5 mL in 1 BOTTLE, DROPPER (63083-9306-1)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): Thio Combination 9306Suffix: 9306
Generic name (nonproprietary): thio combination
Active ingredients: Gelsemium sempervirens root — 3 [hp_X]/29.5mLSodium carbonate — 3 [hp_X]/29.5mLStrychnos nux-vomica seed — 6 [hp_X]/29.5mLChelidonium majus whole — 10 [hp_X]/29.5mLAspartame — 12 [hp_X]/29.5mLCyclamic acid — 12 [hp_X]/29.5mLCysteine — 12 [hp_X]/29.5mLSulfur — 12 [hp_X]/29.5mLThioacetamide — 12 [hp_X]/29.5mLMonoethanolamine thioglycolate — 12 [hp_X]/29.5mL
Dosage form: Liquid
Route: Oral
Labeler: Professional Complementary Health Formulas
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)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 63083-9306_cd371a32-e434-441a-9777-39970363c202SPL ID cd371a32-e434-441a-9777-39970363c202SPL set ID 36e84795-bfb4-4483-9a2c-e14131ce1beaUNII 639KR60Q1Q, 45P3261C7T, 269XH13919, 7E889U5RNN, Z0H242BBR1, HN3OFO5036, K848JZ4886, 70FD1KFU70, 075T165X8M, 263SH5220T
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

N463083930601 followed by a unit qualifier and the quantity

Package 63083-9306-01. 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 occasional headache, nasal congestion, shortness of breath, skin irritation, weakness, nausea, or diarrhea.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)