Centrocode NDC 43406-0124

NDC codes

FDA NDC Directory

Product NDC (as listed)43406-0124Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43406-0124Add 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
43406-0124-1	43406012401	30 mL in 1 BOTTLE, DROPPER (43406-0124-1)Marketed from Jan 1, 2010

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): Centrocode
Generic name (nonproprietary): american ginseng, adenosine triphosphate, corticotropin, alfalfa, bos taurus hypothalamus, phytolacca americana root, bos taurus pituitary gland posterior, thyroid unspecified, iodine, silicon dioxide, oster shell calcium carbonate crude, strychnos ignatii seed, iridium, lachesis muta venom, lycopodium clavatum spore, sodium chloride, strychnos nux-vomica seed, phosphorus, selenium, uranyl nitrate hexahydrate.
Active ingredients: American ginseng — 3 [hp_X]/mLAdenosine triphosphate — 6 [hp_X]/mLCorticotropin — 6 [hp_X]/mLAlfalfa — 6 [hp_X]/mLBos taurus hypothalamus — 6 [hp_X]/mLPhytolacca americana root — 6 [hp_X]/mLBos taurus pituitary gland, Posterior — 6 [hp_X]/mLThyroid, Unspecified — 6 [hp_X]/mLIodine — 12 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mLOyster shell calcium carbonate, Crude — 30 [hp_C]/mLStrychnos ignatii seed — 30 [hp_C]/mLIridium — 30 [hp_C]/mLLachesis muta venom — 30 [hp_C]/mLLycopodium clavatum spore — 30 [hp_C]/mLSodium chloride — 30 [hp_C]/mLStrychnos nux-vomica seed — 30 [hp_C]/mLPhosphorus — 30 [hp_C]/mLSelenium — 30 [hp_C]/mLUranyl nitrate hexahydrate — 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: Jan 1, 2010
Listing expires: Dec 31, 2026
Other FDA classes: Adrenocorticotropic Hormone (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 43406-0124_3d257ccd-5bd0-462c-a9b3-76b7224f484eSPL ID 3d257ccd-5bd0-462c-a9b3-76b7224f484eSPL set ID e5bbe9ec-7602-4de5-907a-7047c10198b6UNII 8W75VCV53Q, 8L70Q75FXE, K0U68Q2TXA, DJO934BRBD, S6G2NLH4Y7, 11E6VI8VEG, 7JM57I419K, 0B4FDL9I6P, 9679TC07X4, ETJ7Z6XBU4, 2E32821G6I, 1NM3M2487K, 44448S9773, VSW71SS07I, C88X29Y479, 451W47IQ8X, 269XH13919, 27YLU75U4W, H6241UJ22B, 3V057702FYUPC 0877730000828
Pharmacologic class: Adrenocorticotropic Hormone; 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

N443406012401 followed by a unit qualifier and the quantity

Package 43406-0124-01. 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

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