What is NDC 73296-019?

73296-019 is the product NDC for Hypericum Perforatum 30X (hypericum perforatum), Hypericum perforatum whole 30 [hp_X]/g globule, listed with the FDA by Laboratoire Schmidt-Nagel Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Hypericum Perforatum 30X (Hypericum Perforatum).

Laboratoire Schmidt-Nagel Inc., NDC labeler code 73296. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Hypericum Perforatum 30X?

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.

Hypericum Perforatum 30X NDC 73296-019

NDC codes

FDA NDC Directory

Product NDC (as listed)73296-019Labeler and product segments. Claims need a package NDC.

Product NDC at billing width73296-0019Add 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
73296-019-01	7329600190173296001901	4 g in 1 TUBE (73296-019-01)Marketed from May 1, 2025

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): Hypericum Perforatum 30X
Generic name (nonproprietary): hypericum perforatum
Active ingredients: Hypericum perforatum whole — 30 [hp_X]/g
Dosage form: Globule
Route: Oral, Sublingual
Labeler: Laboratoire Schmidt-Nagel Inc.NDC labeler code 73296
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 1, 2025
Listing expires: Dec 31, 2026
Identifiers: Product ID 73296-019_3593a7ff-b424-dcfe-e063-6394a90ad0afSPL ID 3593a7ff-b424-dcfe-e063-6394a90ad0afSPL set ID 3363ee64-2f54-1467-e063-6294a90a2a4dUNII XK4IUX8MNB

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

NDC on a medical claim

N473296001901 followed by a unit qualifier and the quantity

Package 73296-0019-01. 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 May 20, 2025.

Indications (excerpt from the label)

For nerve pain after surgery or injury*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 73296-019

What is NDC 73296-019?: 73296-019 is the product NDC for Hypericum Perforatum 30X (hypericum perforatum), Hypericum perforatum whole 30 [hp_X]/g globule, listed with the FDA by Laboratoire Schmidt-Nagel Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Hypericum Perforatum 30X (Hypericum Perforatum).
What is the active ingredient?: Hypericum perforatum whole.
Who is the labeler?: Laboratoire Schmidt-Nagel Inc., NDC labeler code 73296. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Hypericum Perforatum 30X?: 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.

Hypericum Perforatum 30X (Hypericum perforatum) NDC 73296-019