Headache NDC 55714-2598

NDC codes

FDA NDC Directory

Product NDC (as listed)55714-2598Labeler and product segments. Claims need a package NDC.

Product NDC at billing width55714-2598Add 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
55714-2598-1	55714259801	28 g in 1 BOTTLE, GLASS (55714-2598-1)Marketed from Dec 2, 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): Headache
Generic name (nonproprietary): elaps corallinus, arsenicum alb., belladonna, bryonia, carduus benedictus, cimicifuga, coffea cruda, convallaria, crotalus horridus, digitalis, gelsemium, glonoinum, ignatia, lachesis, merc. viv., naja, nux vom., phosphorus, rhus toxicodendron, sanguinaria, secale, vipera berus, apis mel., hypericum, thuja occ..
Active ingredients: Micrurus corallinus venom — 30 [hp_X]/gArsenic trioxide — 15 [hp_X]/gAtropa belladonna — 15 [hp_X]/gBryonia alba root — 15 [hp_X]/gCentaurea benedicta — 15 [hp_X]/gBlack cohosh — 15 [hp_X]/gArabica coffee bean — 15 [hp_X]/gConvallaria majalis — 15 [hp_X]/gCrotalus horridus horridus venom — 15 [hp_X]/gDigitalis — 15 [hp_X]/gGelsemium sempervirens root — 15 [hp_X]/gNitroglycerin — 15 [hp_X]/gStrychnos ignatii seed — 15 [hp_X]/gLachesis muta venom — 15 [hp_X]/gMercury — 15 [hp_X]/gNaja naja venom — 15 [hp_X]/gStrychnos nux-vomica seed — 15 [hp_X]/gPhosphorus — 15 [hp_X]/gToxicodendron pubescens leaf — 15 [hp_X]/gSanguinaria canadensis root — 15 [hp_X]/gClaviceps purpurea sclerotium — 15 [hp_X]/gVipera berus venom — 16 [hp_X]/gApis mellifera — 6 [hp_X]/gHypericum perforatum — 6 [hp_X]/gThuja occidentalis leafy twig — 6 [hp_X]/g
Dosage form: Pellet
Route: Oral
Labeler: Newton Laboratories, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 2, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Nitrates (Chemical structure)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Vasodilation (Physiologic effect)
Identifiers: Product ID 55714-2598_44ffb50a-7bff-428b-e063-6394a90a9dcfSPL ID 44ffb50a-7bff-428b-e063-6394a90a9dcfSPL set ID 44ffb50a-7bfe-428b-e063-6394a90a9dcfUNII V0S6H36980, S7V92P67HO, WQZ3G9PF0H, T7J046YI2B, 6L5ZL09795, K73E24S6X9, 3SW678MX72, QHH4HVF5QE, YHA2XLJ956, F1T8QT9U8B, 639KR60Q1Q, G59M7S0WS3, 1NM3M2487K, VSW71SS07I, FXS1BY2PGL, ZZ4AG7L7VM, 269XH13919, 27YLU75U4W, 6IO182RP7A, N9288CD508, 01G9XEA93N, 0ORO6NCA4M, 7S82P3R43Z, XK4IUX8MNB, 1NT28V9397
Pharmacologic class: Nitrate Vasodilator; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; 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

N455714259801 followed by a unit qualifier and the quantity

Package 55714-2598-01. 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 Dec 2, 2025.

Indications (excerpt from the label)

INDICATIONS & USAGE SECTION Formulated for associated symptoms such as throbbing pain, pressure, congestion, dizziness, nausea and light sensitivity.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)