What is NDC 44911-0209?

44911-0209 is the product NDC for Aconite (aconitum napellus), Aconitum napellus whole 200 [hp_C]/mL liquid, listed with the FDA by ENERGIQUE, INC.. It has 1 package NDC, shown above in 10- and 11-digit form.

ENERGIQUE, INC., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Aconite?

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.

Aconite NDC 44911-0209 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0209Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0209Add 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
44911-0209-1	4491102090144911020901	30 mL in 1 BOTTLE, DROPPER (44911-0209-1)Marketed from Jul 15, 2015

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): Aconite
Generic name (nonproprietary): aconitum napellus
Active ingredients: Aconitum napellus whole — 200 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: ENERGIQUE, INC.NDC labeler code 44911
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 15, 2015
Listing expires: Dec 31, 2026
Identifiers: Product ID 44911-0209_04259ae1-7e7d-4018-9866-9b0f378b2cfcSPL ID 04259ae1-7e7d-4018-9866-9b0f378b2cfcSPL set ID e5f8aa8c-0764-49e8-a2b1-4b8291eef882UNII U0NQ8555JD

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

N444911020901 followed by a unit qualifier and the quantity

Package 44911-0209-01. 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 Jun 7, 2023.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve sudden onset of illness with intense pain.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 44911-0209

What is NDC 44911-0209?: 44911-0209 is the product NDC for Aconite (aconitum napellus), Aconitum napellus whole 200 [hp_C]/mL liquid, listed with the FDA by ENERGIQUE, INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Aconite (Aconitum napellus).
What is the active ingredient?: Aconitum napellus whole.
Who is the labeler?: ENERGIQUE, INC., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Aconite?: 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.

Aconite (Aconitum napellus) NDC 44911-0209