Cerebromax NDC 43742-1486

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1486Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1486Add 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
43742-1486-1	43742148601	30 mL in 1 BOTTLE, DROPPER (43742-1486-1)Marketed from May 17, 2019

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): Cerebromax
Generic name (nonproprietary): acetylcholine chloride, taurine, adenosinum cyclophosphoricum, cerebrum suis, diencephalon (suis), pineal gland (suis), thalamus opticus (suis), adrenalinum, dopamine hydrochloride, gaba (gamma-aminobutyric acid), norepinephrine (bitartrate), serotonin (hydrochloride), tyramine
Active ingredients: Acetylcholine chloride — 6 [hp_X]/mLTaurine — 6 [hp_X]/mLAdenosine cyclic phosphate — 8 [hp_X]/mLSus scrofa cerebrum — 8 [hp_X]/mLSus scrofa diencephalon — 8 [hp_X]/mLSus scrofa pineal gland — 8 [hp_X]/mLSus scrofa thalamus lateral geniculate nucleus — 8 [hp_X]/mLEpinephrine — 8 [hp_X]/mLDopamine hydrochloride — 8 [hp_X]/mL.gamma.-aminobutyric acid — 8 [hp_X]/mLNorepinephrine bitartrate — 8 [hp_X]/mLSerotonin hydrochloride — 8 [hp_X]/mLTyramine — 8 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 17, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Adrenergic alpha-Agonists (Mechanism)Adrenergic beta-Agonists (Mechanism)Catecholamines (Chemical structure)Catecholamines (Chemical structure)Catecholamines (Chemical structure)Cholinergic Agonists (Mechanism)
Identifiers: Product ID 43742-1486_c08b79e3-efe8-4338-91cb-e8526eab5654SPL ID c08b79e3-efe8-4338-91cb-e8526eab5654SPL set ID 39cb1539-7e17-4e9c-96e8-01e5bf584084UNII AF73293C2R, 1EQV5MLY3D, E0399OZS9N, 4GB5DQR532, 23PJ4252VL, 050QZ2EDK7, P146I3107T, YKH834O4BH, 7L3E358N9L, 2ACZ6IPC6I, IFY5PE3ZRW, GKN429M9VS, X8ZC7V0OX3UPC 0810151880808
Pharmacologic class: Catecholamine; Cholinergic Receptor Agonist; alpha-Adrenergic Agonist; beta-Adrenergic Agonist

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

N443742148601 followed by a unit qualifier and the quantity

Package 43742-1486-01. 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 Feb 19, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms related to: • emotional problems • sleep problems • memory problems These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)