What is NDC 71919-773?

71919-773 is the product NDC for Bellis Perennis Kit Refill (bellis perennis), Bellis perennis 200 [hp_C]/1 pellet, listed with the FDA by Washington Homeopathic Products. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Bellis Perennis Kit Refill (Bellis perennis).

Washington Homeopathic Products, NDC labeler code 71919. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Bellis Perennis Kit Refill?

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.

Bellis Perennis Kit Refill NDC 71919-773

NDC codes

FDA NDC Directory

Product NDC (as listed)71919-773Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71919-0773Add 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
71919-773-01	7191907730171919077301	350 PELLET in 1 VIAL, GLASS (71919-773-01)Marketed from Jun 10, 2022

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): Bellis Perennis Kit Refill
Generic name (nonproprietary): bellis perennis
Active ingredients: Bellis perennis — 200 [hp_C]/1
Dosage form: Pellet
Route: Oral
Labeler: Washington Homeopathic ProductsNDC labeler code 71919
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 10, 2022
Listing expires: Dec 31, 2026
Identifiers: Product ID 71919-773_2cc7e78c-a576-f042-e063-6394a90ad14cSPL ID 2cc7e78c-a576-f042-e063-6394a90ad14cSPL set ID e11a653d-42d4-1b82-e053-2a95a90a3b58UNII 2HU33I03UY

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

N471919077301 followed by a unit qualifier and the quantity

Package 71919-0773-01. 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 28, 2025.

Indications (excerpt from the label)

INDICATIONS Indications: BELLIS PERENNIS Bruised soreness

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71919-773

What is NDC 71919-773?: 71919-773 is the product NDC for Bellis Perennis Kit Refill (bellis perennis), Bellis perennis 200 [hp_C]/1 pellet, listed with the FDA by Washington Homeopathic Products. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Bellis Perennis Kit Refill (Bellis perennis).
What is the active ingredient?: Bellis perennis.
Who is the labeler?: Washington Homeopathic Products, NDC labeler code 71919. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Bellis Perennis Kit Refill?: 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.

Bellis Perennis Kit Refill (Bellis perennis) NDC 71919-773