Lymphastat V NDC 44911-0657

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0657Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0657Add 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
44911-0657-1	44911065701	30 mL in 1 BOTTLE, DROPPER (44911-0657-1)Marketed from Jul 20, 2022

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 VSuffix: V
Generic name (nonproprietary): echinacea (angustifolia), lomatium dissectum, hydrastis canadensis, sambucus nigra, aconitum napellus, anas barbariae, hepatis et cordis extractum, arsenicum album, belladonna, bryonia (alba), eupatorium perfoliatum, gelsemium sempervirens, influenzinum (2021-2022), lachesis mutus, rhus tox, pyrogenium
Active ingredients: Echinacea angustifolia whole — 3 [hp_X]/mLLomatium dissectum root — 3 [hp_X]/mLGoldenseal — 6 [hp_X]/mLSambucus nigra flowering top — 6 [hp_X]/mLAconitum napellus whole — 12 [hp_X]/mLCairina moschata heart/liver autolysate — 12 [hp_X]/mLArsenic trioxide — 12 [hp_X]/mLAtropa belladonna — 12 [hp_X]/mLBryonia alba root — 12 [hp_X]/mLEupatorium perfoliatum flowering top — 12 [hp_X]/mLGelsemium sempervirens root — 12 [hp_X]/mLInfluenza a virus a/victoria/2570/2019 ivr-215 (H1n1) antigen (Formaldehyde inactivated) — 12 [hp_X]/mLInfluenza a virus a/tasmania/503/2020 ivr-221 (H3n2) antigen (Formaldehyde inactivated) — 12 [hp_X]/mLInfluenza b virus b/washington/02/2019 antigen (Formaldehyde inactivated) — 12 [hp_X]/mLInfluenza b virus b/phuket/3073/2013 antigen (Formaldehyde inactivated) — 12 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLToxicodendron pubescens leaf — 12 [hp_X]/mLRancid beef — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 20, 2022
Marketing end: Sep 8, 2027
Identifiers: Product ID 44911-0657_92365727-70fe-4c1e-bac2-4d58a6948cd2SPL ID 92365727-70fe-4c1e-bac2-4d58a6948cd2SPL set ID 9ec6f663-5f15-4daf-a36b-49fbe1c53a6cUNII VB06AV5US8, 5329928G5N, ZW3Z11D0JV, CT03BSA18U, U0NQ8555JD, RN2HC612GY, S7V92P67HO, WQZ3G9PF0H, T7J046YI2B, 1W0775VX6E, 639KR60Q1Q, WD5E5VYM2E, V529EJB2CX, VEH9U90EHX, B93BQX9789, VSW71SS07I, 6IO182RP7A, 29SUH5R3HU

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

N444911065701 followed by a unit qualifier and the quantity

Package 44911-0657-01. 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 Mar 11, 2025.

Indications (excerpt from the label)

INDICATIONS: May temporary relieve fever, runny nose, achiness, or rash.** **Claims based on traditional homeopathic practice. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)