What is NDC 63083-7140?

63083-7140 is the product NDC for Thuja occidentalis 7140 (thuja occidentalis), Thuja occidentalis leaf 6 [hp_X]/29.5mL 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?

Thuja occidentalis 7140 (Thuja occidentalis).

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 Thuja occidentalis 7140?

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.

Thuja occidentalis 7140 NDC 63083-7140

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-7140Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-7140Add 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
63083-7140-1	63083714001	29.5 mL in 1 BOTTLE, DROPPER (63083-7140-1)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): Thuja occidentalis 7140Suffix: 7140
Generic name (nonproprietary): thuja occidentalis
Active ingredients: Thuja occidentalis leaf — 6 [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
Identifiers: Product ID 63083-7140_94dc8bd9-ad89-4893-ad88-cd3bfcb2260aSPL ID 94dc8bd9-ad89-4893-ad88-cd3bfcb2260aSPL set ID 11364528-399d-4f64-a682-ec8f503af0aaUNII 0T0DQN8786

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

N463083714001 followed by a unit qualifier and the quantity

Package 63083-7140-01. 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 Use according to standard homeopathic indications for self-limiting conditions. Common Materia Medica indications: warts, headache, exhaustion, cramps.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63083-7140

What is NDC 63083-7140?: 63083-7140 is the product NDC for Thuja occidentalis 7140 (thuja occidentalis), Thuja occidentalis leaf 6 [hp_X]/29.5mL 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?: Thuja occidentalis 7140 (Thuja occidentalis).
What is the active ingredient?: Thuja occidentalis leaf.
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 Thuja occidentalis 7140?: 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.

Thuja occidentalis 7140 (Thuja occidentalis) NDC 63083-7140