Dynamic Brain NDC 43742-1451

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1451Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1451Add 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
43742-1451-1	43742145101	30 mL in 1 BOTTLE, DROPPER (43742-1451-1)Marketed from Mar 15, 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): Dynamic Brain
Generic name (nonproprietary): argentum nitricum, cuprum aceticum, ginkgo biloba, kali phosphoricum, lycopodium clavatum, phosphoricum acidum, thiaminum hydrochloricum, cerebrum suis, ambra grisea, picricum acidum, agnus castus, alumina, anacardium orientale, baryta carbonica, cicuta virosa, conium maculatum, helleborus niger, plumbum metallicum, selenium metallicum, zincum metallicum
Active ingredients: Silver nitrate — 6 [hp_X]/mLCupric acetate — 6 [hp_X]/mLGinkgo — 6 [hp_X]/mLDibasic potassium phosphate — 6 [hp_X]/mLLycopodium clavatum spore — 6 [hp_X]/mLPhosphoric acid — 6 [hp_X]/mLThiamine hydrochloride — 6 [hp_X]/mLSus scrofa cerebrum — 8 [hp_X]/mLAmbergris — 9 [hp_X]/mLPicric acid — 10 [hp_X]/mLChaste tree fruit — 12 [hp_X]/mLAluminum oxide — 12 [hp_X]/mLSemecarpus anacardium juice — 12 [hp_X]/mLBarium carbonate — 12 [hp_X]/mLCicuta virosa root — 12 [hp_X]/mLConium maculatum flowering top — 12 [hp_X]/mLHelleborus niger root — 12 [hp_X]/mLLead — 12 [hp_X]/mLSelenium — 12 [hp_X]/mLZinc — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 15, 2019
Listing expires: Dec 31, 2027
Identifiers: Product ID 43742-1451_39e754a6-9237-432a-8406-6f0596cd8192SPL ID 39e754a6-9237-432a-8406-6f0596cd8192SPL set ID 60a1e44b-3f91-41de-82c2-4648fb800dcdUNII 95IT3W8JZE, 39M11XPH03, 19FUJ2C58T, CI71S98N1Z, C88X29Y479, E4GA8884NN, M572600E5P, 4GB5DQR532, XTC0D02P6C, A49OS0F91S, 433OSF3U8A, LMI26O6933, Y0F0BU8RDU, 6P669D8HQ8, YEA9P21S8N, Q28R5GF371, 608DGJ6815, 2P299V784P, H6241UJ22B, J41CSQ7QDSUPC 0810151883717

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

N443742145101 followed by a unit qualifier and the quantity

Package 43742-1451-01. 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 Mar 19, 2026.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • forgetfulness • confusion • absent mindedness • dullness 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)