What is NDC 71919-812?

71919-812 is the product NDC for Antimonium Crudum Kit Refill (antimony trisulfide), Antimony trisulfide 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?

Antimonium Crudum Kit Refill (Antimony trisulfide).

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 Antimonium Crudum 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.

Antimonium Crudum Kit Refill NDC 71919-812

NDC codes

FDA NDC Directory

Product NDC (as listed)71919-812Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71919-0812Add 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
71919-812-01	7191908120171919081201	750 PELLET in 1 VIAL, GLASS (71919-812-01)Marketed from Nov 7, 2023

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): Antimonium Crudum Kit Refill
Generic name (nonproprietary): antimony trisulfide
Active ingredients: Antimony trisulfide — 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: Nov 7, 2023
Listing expires: Dec 31, 2026
Identifiers: Product ID 71919-812_2cc87194-4ca1-f4af-e063-6294a90a596bSPL ID 2cc87194-4ca1-f4af-e063-6294a90a596bSPL set ID 0991be25-8930-3c09-e063-6294a90ac5e2UNII F79059A38U

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

N471919081201 followed by a unit qualifier and the quantity

Package 71919-0812-01. 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: ANTIMONIUM CRUDUM Warts

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71919-812

What is NDC 71919-812?: 71919-812 is the product NDC for Antimonium Crudum Kit Refill (antimony trisulfide), Antimony trisulfide 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?: Antimonium Crudum Kit Refill (Antimony trisulfide).
What is the active ingredient?: Antimony trisulfide.
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 Antimonium Crudum 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.

Antimonium Crudum Kit Refill (Antimony trisulfide) NDC 71919-812