Headache NDC 43857-0805

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0805Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0805Add 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
43857-0805-1	43857080501	30 mL in 1 BOTTLE, DROPPER (43857-0805-1)Marketed from Sep 10, 2026

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): melilotus officinalis, spigelia anthelmia, allium cepa, belladonna, bryonia (alba), cimicifuga racemosa, gelsemium sempervirens, glonoinum, lachesis mutus, magnesia phosphorica, nux vomica, sanguinaria canadensis, silicea
Active ingredients: Melilotus officinalis top — 3 [hp_X]/mLSpigelia anthelmia whole — 6 [hp_X]/mLOnion — 12 [hp_X]/mLAtropa belladonna — 12 [hp_X]/mLBryonia alba root — 12 [hp_X]/mLBlack cohosh — 12 [hp_X]/mLNitroglycerin — 12 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLMagnesium phosphate, Dibasic trihydrate — 12 [hp_X]/mLStrychnos nux-vomica seed — 12 [hp_X]/mLSanguinaria canadensis root — 12 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritionals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 10, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)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 IgG Production (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Nitrates (Chemical structure)Osmotic Activity (Mechanism)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)Vasodilation (Physiologic effect)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 43857-0805_489b6206-2643-405d-bdc9-b8aa814bf74cSPL ID 489b6206-2643-405d-bdc9-b8aa814bf74c
Pharmacologic class: Calculi Dissolution Agent; Nitrate Vasodilator; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Osmotic Laxative

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

N443857080501 followed by a unit qualifier and the quantity

Package 43857-0805-01. 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

The FDA listing for this product does not reference a label (SPL) set.