What is NDC 76472-3039?

76472-3039 is the product NDC for THUJA OCCIDENTALIS 200ck (thuja occidentalis), Thuja occidentalis bark 200 [kp_C]/1 pellet, listed with the FDA by SEVENE USA. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

THUJA OCCIDENTALIS 200ck (Thuja occidentalis).

SEVENE USA, NDC labeler code 76472. 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 200ck?

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 200ck NDC 76472-3039

NDC codes

FDA NDC Directory

Product NDC (as listed)76472-3039Labeler and product segments. Claims need a package NDC.

Product NDC at billing width76472-3039Add 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
76472-3039-1	76472303901	80 PELLET in 1 CYLINDER (76472-3039-1)Marketed from Nov 23, 2011

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 200ckSuffix: 200ck
Generic name (nonproprietary): thuja occidentalis
Active ingredients: Thuja occidentalis bark — 200 [kp_C]/1
Dosage form: Pellet
Route: Sublingual
Labeler: SEVENE USANDC labeler code 76472
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 23, 2011
Listing expires: Dec 31, 2026
Identifiers: Product ID 76472-3039_2dcc6766-0ad5-3099-e063-6394a90ae3cbSPL ID 2dcc6766-0ad5-3099-e063-6394a90ae3cbSPL set ID cf8a98e7-ab41-bcc4-e053-2995a90ad8bdUNII 19RAD88E6OUPC 0810095311581

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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N476472303901 followed by a unit qualifier and the quantity

Package 76472-3039-01. 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 Feb 10, 2025.

Indications (excerpt from the label)

USE Condition listed above or as directed by a physician.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 76472-3039

What is NDC 76472-3039?: 76472-3039 is the product NDC for THUJA OCCIDENTALIS 200ck (thuja occidentalis), Thuja occidentalis bark 200 [kp_C]/1 pellet, listed with the FDA by SEVENE USA. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: THUJA OCCIDENTALIS 200ck (Thuja occidentalis).
What is the active ingredient?: Thuja occidentalis bark.
Who is the labeler?: SEVENE USA, NDC labeler code 76472. 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 200ck?: 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 200ck (Thuja occidentalis) NDC 76472-3039