NDC codes

FDA NDC Directory
Product NDC (as listed)44911-0707Labeler and product segments. Claims need a package NDC.
Product NDC at billing width44911-0707Add 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 NDC11-digit (billing)PackageCopy
44911-0707-14491107070130 mL in 1 BOTTLE, DROPPER (44911-0707-1)Marketed from Sep 20, 2024

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), 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
Active ingredients
Echinacea angustifolia whole — 3 [hp_X]/mLCalendula officinalis flowering top — 6 [hp_X]/mLSus scrofa lymph — 6 [hp_X]/mLPhytolacca americana root — 6 [hp_X]/mLAsterias rubens — 12 [hp_X]/mLBarium carbonate — 12 [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]/mLScrophularia nodosa whole — 12 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mL
Dosage form
Liquid
Route
Oral
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
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 44911-0707_f5d9b526-5d60-4e1a-b4e9-6bb228b4f4ffSPL ID f5d9b526-5d60-4e1a-b4e9-6bb228b4f4ffSPL set ID db485f2b-a5d9-49ac-b3ba-bcc0256961edUNII VB06AV5US8, 18E7415PXQ, 33A7VYU29L, 11E6VI8VEG, A7FYY9Q742, 6P669D8HQ8, Q28R5GF371, F5452U54PN, 1MBW07J51Q, 660YQ98I10, VSW71SS07I, 7H443NUB2T, 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

N444911070701 followed by a unit qualifier and the quantity

Package 44911-0707-01. 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 .

Indications (excerpt from the label)

USES: May temporarily relieve: •swollen tonsils •irritated throat 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)

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