NDC codes

FDA NDC Directory
Product NDC (as listed)43857-0657Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43857-0657Add 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 NDC11-digit (billing)PackageCopy
43857-0657-14385706570160 mL in 1 BOTTLE, DROPPER (43857-0657-1)Marketed from Jun 3, 2025

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 Tonic ISuffix: I
Generic name (nonproprietary)
echinacea (angustifolia), kali iodatum, phytolacca decandra, pinus sylvestris, hypophysis suis, apis mellifica, aranea diadema, belladonna, calcarea carbonica, clematis erecta, conium maculatum, galium aparine, graphites, lachesis mutus, mercurius praecipitatus ruber, myristica sebifera, phosphorus, rhus tox, scrophularia nodosa, sulphur, thyroidinum (suis), vespa crabro
Active ingredients
Echinacea angustifolia whole — 1 [hp_X]/mLPotassium iodide — 3 [hp_X]/mLPhytolacca americana root — 4 [hp_X]/mLPinus sylvestris leafy twig — 6 [hp_X]/mLSus scrofa pituitary gland — 8 [hp_X]/mLApis mellifera — 12 [hp_X]/mLAraneus diadematus — 12 [hp_X]/mLAtropa belladonna — 12 [hp_X]/mLOyster shell calcium carbonate, Crude — 12 [hp_X]/mLClematis recta flowering top — 12 [hp_X]/mLConium maculatum flowering top — 12 [hp_X]/mLGalium aparine whole — 12 [hp_X]/mLGraphite — 12 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLMercuric oxide — 12 [hp_X]/mLVirola sebifera resin — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLToxicodendron pubescens leaf — 12 [hp_X]/mLScrophularia nodosa whole — 12 [hp_X]/mLSulfur — 12 [hp_X]/mLThyroid — 12 [hp_X]/mLVespa crabro — 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
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 43857-0657_6a8125ab-da03-4d44-a9c9-81ed6485ee54SPL ID 6a8125ab-da03-4d44-a9c9-81ed6485ee54SPL set ID 9b9a639c-0a91-48b5-b1ff-6b82c6a568efUNII VB06AV5US8, 1C4QK22F9J, 11E6VI8VEG, Q1RGP4UB73, L0PFEMQ1DT, 7S82P3R43Z, 6T6CO7R3Z5, WQZ3G9PF0H, 2E32821G6I, 396421SP9F, Q28R5GF371, Z4B6561488, 4QQN74LH4O, VSW71SS07I, IY191986AO, GHJ5XX5SGS, 27YLU75U4W, 6IO182RP7A, 7H443NUB2T, 70FD1KFU70, 6RV024OAUQ, K3ALM8S49H
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

N443857065701 followed by a unit qualifier and the quantity

Package 43857-0657-01. 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 .

Indications (excerpt from the label)

USES: For temporary relief of glandular swelling with inflammation and induration, glands hot, swollen, painful; scrofulous swelling; axillary glands swollen with soreness of the upper arm.** **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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