What is NDC 44911-0456?

44911-0456 is the product NDC for Lymphapar, Echinacea angustifolia 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?

Lymphapar (Echinacea (Angustifolia), Lymph Node (Suis), Phytolacca Decandra, Conium Maculatum, Ferrum Iodatum, Hepar Sulphuris Calcareum , Kali Muriaticum, Lachesis Mutus, Silicea).

What is the active ingredient?

Echinacea angustifolia, Sus scrofa lymph, Phytolacca americana root, Conium maculatum flowering top, Ferrous iodide, Calcium sulfide, Potassium chloride, Lachesis muta venom, Silicon dioxide.

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 Lymphapar?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Lymphapar NDC 44911-0456 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0456Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0456Add 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
44911-0456-1	4491104560144911045601	30 mL in 1 BOTTLE, DROPPER (44911-0456-1)Marketed from May 14, 2018

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): Lymphapar
Generic name (nonproprietary): echinacea (angustifolia), lymph node (suis), phytolacca decandra, conium maculatum, ferrum iodatum, hepar sulphuris calcareum , kali muriaticum, lachesis mutus, silicea
Active ingredients: Echinacea angustifolia — 3 [hp_X]/mLSus scrofa lymph — 6 [hp_X]/mLPhytolacca americana root — 6 [hp_X]/mLConium maculatum flowering top — 12 [hp_X]/mLFerrous iodide — 12 [hp_X]/mLCalcium sulfide — 12 [hp_X]/mLPotassium chloride — 12 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLSilicon dioxide — 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: May 14, 2018
Marketing end: Mar 1, 2027
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)
Identifiers: Product ID 44911-0456_3d25cf38-b872-4a46-b14b-8b09ed77a0a2SPL ID 3d25cf38-b872-4a46-b14b-8b09ed77a0a2SPL set ID c746c111-7ebc-46c1-b11b-04271887df9cUNII VB06AV5US8, 33A7VYU29L, 11E6VI8VEG, Q28R5GF371, F5452U54PN, 1MBW07J51Q, 660YQ98I10, VSW71SS07I, ETJ7Z6XBU4UPC 0363113700572
Pharmacologic class: Osmotic Laxative; 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

N444911045601 followed by a unit qualifier and the quantity

Package 44911-0456-01. 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 Sep 23, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve swollen tonsils or irritated throat and swollen irritated breasts prior to menses.** **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 44911-0456

What is NDC 44911-0456?: 44911-0456 is the product NDC for Lymphapar, Echinacea angustifolia 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?: Lymphapar (Echinacea (Angustifolia), Lymph Node (Suis), Phytolacca Decandra, Conium Maculatum, Ferrum Iodatum, Hepar Sulphuris Calcareum , Kali Muriaticum, Lachesis Mutus, Silicea).
What is the active ingredient?: Echinacea angustifolia, Sus scrofa lymph, Phytolacca americana root, Conium maculatum flowering top, Ferrous iodide, Calcium sulfide, Potassium chloride, Lachesis muta venom, Silicon dioxide.
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 Lymphapar?: 1 other product NDC are listed under this name. See all Lymphapar NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Lymphapar NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Lymphaparechinacea (angustifolia), calendula officinalis, lymph node (suis), phytolacca decandra, asterias rubens, baryta carbonica, conium maculatum, ferrum iodatum, hepar sulphuris calcareum , kali muriaticum, lachesis mutus, scrophularia nodosa, silicea	Echinacea angustifolia whole 3 [hp_X]/mL + 12 more ingredients	LiquidOral	Energique, Inc.	44911-0707	44911-0707-01