Headache HP NDC 43406-0025

NDC codes

FDA NDC Directory

Product NDC (as listed)43406-0025Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43406-0025Add 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
43406-0025-1	43406002501	30 mL in 1 BOTTLE, DROPPER (43406-0025-1)Marketed from May 29, 2007

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 HP
Generic name (nonproprietary): silver nitrate, atropa belladonna, bryonia alba root, gelsemium sempervirens root, nitroglycerin, lachesis muta venom, lycopodium clavatum spore, melilotus officinalis top, sodium chloride, strychnos nux-vomica seed, silicon dioxide, spigelia anthelmia
Active ingredients: Silver nitrate — 30 [hp_C]/mLAtropa belladonna — 30 [hp_C]/mLBryonia alba root — 30 [hp_C]/mLNitroglycerin — 30 [hp_C]/mLLachesis muta venom — 30 [hp_C]/mLLycopodium clavatum spore — 30 [hp_C]/mLMelilotus officinalis top — 30 [hp_C]/mLSodium chloride — 30 [hp_C]/mLStrychnos nux-vomica seed — 30 [hp_C]/mLSilicon dioxide — 30 [hp_C]/mLSpigelia anthelmia — 30 [hp_C]/mL
Dosage form: Liquid
Route: Oral
Labeler: Natural Creations, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 29, 2007
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Nitrates (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Vasodilation (Physiologic effect)
Identifiers: Product ID 43406-0025_f44b45b5-cfa8-4d2d-a530-f973032c08d1SPL ID f44b45b5-cfa8-4d2d-a530-f973032c08d1SPL set ID c38b83f0-3918-4ef6-8dfd-48fe438e584aUNII 95IT3W8JZE, WQZ3G9PF0H, T7J046YI2B, G59M7S0WS3, VSW71SS07I, C88X29Y479, GM6P02J2DX, 451W47IQ8X, 269XH13919, ETJ7Z6XBU4, WYT05213GEUPC 0877730001535
Pharmacologic class: Nitrate Vasodilator; Non-Standardized Plant 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

N443406002501 followed by a unit qualifier and the quantity

Package 43406-0025-01. 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 12, 2025.

Indications (excerpt from the label)

USES: Temporarily relieves symptoms due to tension and pressure of the head, headache.**

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)