Lymph-Tone I NDC 64578-0179

NDC codes

FDA NDC Directory

Product NDC (as listed)64578-0179Labeler and product segments. Claims need a package NDC.

Product NDC at billing width64578-0179Add 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
64578-0179-1	64578017901	59.1 mL in 1 BOTTLE, DROPPER (64578-0179-1)Marketed from Jul 2, 2015

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): Lymph-Tone ISuffix: I
Generic name (nonproprietary): adenosinum cyclophosphoricum, apis mellifica, aranea diadema, belladonna, boldo, calcarea carbonica, echinacea (angustifolia),galium aparine, glandula suprarenalis suis, hypothalamus (bovine), kali iodatum, phosphorus, phytolacca decandra, pinus sylvestris, pituitarum posterium (bovine), pulsatilla (vulgaris), rhus tox, scrophularia nodosa, sulphur, thyroidinum (bovine)
Active ingredients: Adenosine cyclic phosphate — 12 [hp_X]/mLApis mellifera — 12 [hp_X]/mLAraneus diadematus — 12 [hp_X]/mLAtropa belladonna — 12 [hp_X]/mLPeumus boldus leaf — 4 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLEchinacea angustifolia — 4 [hp_X]/mLGalium aparine — 12 [hp_X]/mLSus scrofa adrenal gland — 9 [hp_X]/mLBos taurus hypothalamus — 12 [hp_X]/mLPotassium iodide — 4 [hp_X]/mLPhosphorus — 12 [hp_X]/mLPhytolacca americana root — 4 [hp_X]/mLPinus sylvestris leafy twig — 9 [hp_X]/mLSus scrofa pituitary gland, Posterior — 12 [hp_X]/mLPulsatilla vulgaris — 12 [hp_X]/mLToxicodendron pubescens leaf — 12 [hp_X]/mLScrophularia nodosa — 12 [hp_X]/mLSulfur — 12 [hp_X]/mLThyroid, Unspecified — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energetix Corporation
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 2, 2015
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 64578-0179_39fc87f1-17ef-1e05-e063-6394a90abdc1SPL ID 39fc87f1-17ef-1e05-e063-6394a90abdc1SPL set ID 3fc5510e-38cb-47a5-9858-ea911c9effd7UNII E0399OZS9N, 7S82P3R43Z, 6T6CO7R3Z5, WQZ3G9PF0H, Q4EWM09M3O, 2E32821G6I, VB06AV5US8, Z4B6561488, 398IYQ16YV, S6G2NLH4Y7, 1C4QK22F9J, 27YLU75U4W, 11E6VI8VEG, Q1RGP4UB73, E8S87O660T, I76KB35JEV, 6IO182RP7A, 7H443NUB2T, 70FD1KFU70, 0B4FDL9I6P
Pharmacologic class: Standardized Insect Venom Allergenic Extract

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

N464578017901 followed by a unit qualifier and the quantity

Package 64578-0179-01. 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 Jul 15, 2025.

Indications (excerpt from the label)

Uses Temporary relief of nasal discharge, fever, itching skin.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)