Lymphastat B NDC 44911-0617

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0617Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0617Add 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
44911-0617-1	44911061701	60 mL in 1 BOTTLE, DROPPER (44911-0617-1)Marketed from May 24, 2021

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): Lymphastat B
Generic name (nonproprietary): baptisia tinctoria, echinacea (angustifolia), phytolacca decandra, aconitum napellus, arsenicum album, belladonna, ferrum phosphoricum, lachesis mutus, phosphorus
Active ingredients: Baptisia tinctoria root — 3 [hp_X]/mLEchinacea angustifolia whole — 3 [hp_X]/mLPhytolacca americana root — 6 [hp_X]/mLAconitum napellus — 12 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLAtropa belladonna — 12 [hp_X]/mLFerrosoferric phosphate — 12 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 24, 2021
Marketing end: Jan 11, 2027
Identifiers: Product ID 44911-0617_dd9b5159-7800-4482-a11c-1b0f85326798SPL ID dd9b5159-7800-4482-a11c-1b0f85326798SPL set ID 3a1f761e-eb12-41d8-b185-46da39497b08UNII 5EF0HWI5WU, VB06AV5US8, 11E6VI8VEG, U0NQ8555JD, S7V92P67HO, WQZ3G9PF0H, 91GQH8I5F7, VSW71SS07I, 27YLU75U4WUPC 0363113701197

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

N444911061701 followed by a unit qualifier and the quantity

Package 44911-0617-01. 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 10, 2023.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve fever, irritated throat, and acute irritation of the bladder.** **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)