What is NDC 44911-0181?

44911-0181 is the product NDC for Vertitone, Baptisia tinctoria root 3 [hp_X]/mL + 8 more ingredients 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?

Vertitone (Baptisia Tinctoria, Agaricus Muscarius, Arsenicum Album, Belladonna, Calcarea Carbonica, Cocculus Indicus, Conium Maculatum, Phosphorus, Pulsatilla (Pratensis)).

What is the active ingredient?

Baptisia tinctoria root, Amanita muscaria fruiting body, Arsenic trioxide, Atropa belladonna, Oyster shell calcium carbonate, Crude, Anamirta cocculus seed, Conium maculatum flowering top, Phosphorus, Pulsatilla pratensis whole.

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 Vertitone?

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.

Vertitone NDC 44911-0181 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0181Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0181Add 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
44911-0181-1	4491101810144911018101	30 mL in 1 BOTTLE, DROPPER (44911-0181-1)Marketed from Jul 8, 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): Vertitone
Generic name (nonproprietary): baptisia tinctoria, agaricus muscarius, arsenicum album, belladonna, calcarea carbonica, cocculus indicus, conium maculatum, phosphorus, pulsatilla (pratensis)
Active ingredients: Baptisia tinctoria root — 3 [hp_X]/mLAmanita muscaria fruiting body — 12 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLAtropa belladonna — 12 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLAnamirta cocculus seed — 12 [hp_X]/mLConium maculatum flowering top — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLPulsatilla pratensis whole — 12 [hp_X]/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 8, 2015
Listing expires: Dec 31, 2026
Identifiers: Product ID 44911-0181_2f9df577-5024-4911-9ab7-ad3387dff794SPL ID 2f9df577-5024-4911-9ab7-ad3387dff794SPL set ID 12f1c465-b64a-446c-a28c-e96dabe03580UNII 5EF0HWI5WU, DIF093I037, S7V92P67HO, WQZ3G9PF0H, 2E32821G6I, 810258W28U, Q28R5GF371, 27YLU75U4W, 8E272251DIUPC 0363113700862

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

N444911018101 followed by a unit qualifier and the quantity

Package 44911-0181-01. 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 Oct 31, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve dizziness and motion sickness with nausea.** **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 44911-0181

What is NDC 44911-0181?: 44911-0181 is the product NDC for Vertitone, Baptisia tinctoria root 3 [hp_X]/mL + 8 more ingredients 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?: Vertitone (Baptisia Tinctoria, Agaricus Muscarius, Arsenicum Album, Belladonna, Calcarea Carbonica, Cocculus Indicus, Conium Maculatum, Phosphorus, Pulsatilla (Pratensis)).
What is the active ingredient?: Baptisia tinctoria root, Amanita muscaria fruiting body, Arsenic trioxide, Atropa belladonna, Oyster shell calcium carbonate, Crude, Anamirta cocculus seed, Conium maculatum flowering top, Phosphorus, Pulsatilla pratensis 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 Vertitone?: 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.