What is NDC 44911-0490?

44911-0490 is the product NDC for Elimitone, Bellis perennis whole 3 [hp_X]/mL + 10 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?

Elimitone (Bellis Perennis, Echinacea (Angustifolia), Trifolium Pratense, Phytolacca Decandra, Arnica Montana, Anas Barbariae, Hepatis et Cordis Extractum, Calcarea Iodata, Kali Muriaticum, Nitricum Acidum, Phosphoricum Acidum, Sulphur Iodatum).

What is the active ingredient?

Bellis perennis whole, Echinacea angustifolia whole, Trifolium pratense flower, Phytolacca americana root, Arnica montana whole, Cairina moschata heart/liver autolysate, Calcium iodide, Potassium chloride, Nitric acid, Phosphoric acid, Sulfur iodide.

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 Elimitone?

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.

Elimitone NDC 44911-0490 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0490Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0490Add 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
44911-0490-1	44911049001	30 mL in 1 BOTTLE, DROPPER (44911-0490-1)Marketed from Mar 19, 2019

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): Elimitone
Generic name (nonproprietary): bellis perennis, echinacea (angustifolia), trifolium pratense, phytolacca decandra, arnica montana, anas barbariae, hepatis et cordis extractum, calcarea iodata, kali muriaticum, nitricum acidum, phosphoricum acidum, sulphur iodatum
Active ingredients: Bellis perennis whole — 3 [hp_X]/mLEchinacea angustifolia whole — 3 [hp_X]/mLTrifolium pratense flower — 3 [hp_X]/mLPhytolacca americana root — 4 [hp_X]/mLArnica montana whole — 12 [hp_X]/mLCairina moschata heart/liver autolysate — 12 [hp_X]/mLCalcium iodide — 12 [hp_X]/mLPotassium chloride — 12 [hp_X]/mLNitric acid — 12 [hp_X]/mLPhosphoric acid — 12 [hp_X]/mLSulfur iodide — 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: Mar 19, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Phosphate Chelating Activity (Mechanism)Potassium Compounds (Chemical structure)
Identifiers: Product ID 44911-0490_55f5a7d5-3d34-498a-ba58-9de044037617SPL ID 55f5a7d5-3d34-498a-ba58-9de044037617SPL set ID bc6352e0-6851-4971-948b-b18da7c1c8b6UNII 2HU33I03UY, VB06AV5US8, 4JS0838828, 11E6VI8VEG, O80TY208ZW, RN2HC612GY, 8EKI9QEE2H, 660YQ98I10, 411VRN1TV4, E4GA8884NN, L6L8KA2AA0UPC 0363113701494
Pharmacologic class: Blood Coagulation Factor; Osmotic Laxative; Phosphate Binder; Potassium Salt

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

N444911049001 followed by a unit qualifier and the quantity

Package 44911-0490-01. 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 24, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve irritated throat, swollen glands, and sore joints and muscles.** **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 44911-0490

What is NDC 44911-0490?: 44911-0490 is the product NDC for Elimitone, Bellis perennis whole 3 [hp_X]/mL + 10 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?: Elimitone (Bellis Perennis, Echinacea (Angustifolia), Trifolium Pratense, Phytolacca Decandra, Arnica Montana, Anas Barbariae, Hepatis et Cordis Extractum, Calcarea Iodata, Kali Muriaticum, Nitricum Acidum, Phosphoricum Acidum, Sulphur Iodatum).
What is the active ingredient?: Bellis perennis whole, Echinacea angustifolia whole, Trifolium pratense flower, Phytolacca americana root, Arnica montana whole, Cairina moschata heart/liver autolysate, Calcium iodide, Potassium chloride, Nitric acid, Phosphoric acid, Sulfur iodide.
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 Elimitone?: 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.