Arteriotone NDC 44911-0230

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0230Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0230Add 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
44911-0230-1	44911023001	30 mL in 1 BOTTLE, DROPPER (44911-0230-1)Marketed from Jul 27, 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): Arteriotone
Generic name (nonproprietary): baptisia tinctoria, cactus grandiflorus, echinacea (angustifolia), adonis vernalis, agnus castus, arnica montana, aurum metallicum, digitalis purpurea, glonoinum, vanadium metallicum
Active ingredients: Baptisia tinctoria root — 3 [hp_X]/mLSelenicereus grandiflorus stem — 3 [hp_X]/mLEchinacea angustifolia whole — 3 [hp_X]/mLAdonis vernalis whole — 12 [hp_X]/mLChaste tree fruit — 12 [hp_X]/mLArnica montana whole — 12 [hp_X]/mLGold — 12 [hp_X]/mLDigitalis — 12 [hp_X]/mLNitroglycerin — 12 [hp_X]/mLVanadium — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 27, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Nitrates (Chemical structure)Vasodilation (Physiologic effect)
Identifiers: Product ID 44911-0230_33a86817-1d07-4e87-90c2-11d12edae391SPL ID 33a86817-1d07-4e87-90c2-11d12edae391SPL set ID 4bb46cf1-bfcb-4d57-a982-7ba87e2b299aUNII 5EF0HWI5WU, 7114SV0MYK, VB06AV5US8, DX3ZNI25WK, 433OSF3U8A, O80TY208ZW, 79Y1949PYO, F1T8QT9U8B, G59M7S0WS3, 00J9J9XKDEUPC 0363113700060
Pharmacologic class: Nitrate Vasodilator; Standardized Chemical Allergen

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

N444911023001 followed by a unit qualifier and the quantity

Package 44911-0230-01. 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 Jul 16, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve symptoms of swollen extremities, bruised feeling, cold clammy feet, mild burning pains in leg, and weakness in limbs.** **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)