What is NDC 0220-0320?

0220-0320 is the product NDC for Anatherum muriaticum (chrysopogon zizanioides root), Chrysopogon zizanioides root 30 [hp_C]/30[hp_C] pellet, listed with the FDA by Boiron. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Anatherum muriaticum (Chrysopogon zizanioides root).

Boiron, NDC labeler code 0220. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Anatherum muriaticum?

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.

Anatherum muriaticum NDC 0220-0320 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)0220-0320Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00220-0320Add 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
0220-0320-41	00220032041	30 [hp_C] in 1 TUBE (0220-0320-41)Marketed from Mar 3, 1983

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Anatherum muriaticum
Generic name (nonproprietary): chrysopogon zizanioides root
Active ingredients: Chrysopogon zizanioides root — 30 [hp_C]/30[hp_C]
Dosage form: Pellet
Route: Oral
Labeler: BoironNDC labeler code 0220
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 3, 1983
Listing expires: Dec 31, 2026
Identifiers: Product ID 0220-0320_1a01f718-3962-fb5d-e063-6394a90a7faaSPL ID 1a01f718-3962-fb5d-e063-6394a90a7faaSPL set ID 6a113bbe-1dce-a585-e053-2a91aa0aa905UNII 37TB8LUP9Z

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

N400220032041 followed by a unit qualifier and the quantity

Package 00220-0320-41. 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 Jun 3, 2024.

Indications (excerpt from the label)

Relieves skin rash * Uses: See symptoms on front panel.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0220-0320

What is NDC 0220-0320?: 0220-0320 is the product NDC for Anatherum muriaticum (chrysopogon zizanioides root), Chrysopogon zizanioides root 30 [hp_C]/30[hp_C] pellet, listed with the FDA by Boiron. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Anatherum muriaticum (Chrysopogon zizanioides root).
What is the active ingredient?: Chrysopogon zizanioides root.
Who is the labeler?: Boiron, NDC labeler code 0220. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Anatherum muriaticum?: 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.

Anatherum muriaticum (Chrysopogon zizanioides root) NDC 0220-0320