Cerebraplex NDC 43857-0398

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0398Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0398Add 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
43857-0398-1	43857039801	30 mL in 1 BOTTLE, DROPPER (43857-0398-1)Marketed from Jun 6, 2016

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): Cerebraplex
Generic name (nonproprietary): avena sativa, capsicum annuum, ginkgo biloba, hydrocotyle asiatica, polygonum multiflorum, rosmarinus officinalis, vinca minor, cerebrum suis, baryta carbonica, belladonna, germanium sesquioxide, kali phosphoricum, stramonium
Active ingredients: Avena sativa flowering top — 3 [hp_X]/mLCapsicum — 3 [hp_X]/mLGinkgo — 3 [hp_X]/mLCentella asiatica whole — 3 [hp_X]/mLFallopia multiflora root — 3 [hp_X]/mLRosmarinus officinalis flowering top — 3 [hp_X]/mLVinca minor whole — 3 [hp_X]/mLSus scrofa cerebrum — 6 [hp_X]/mLBarium carbonate — 12 [hp_X]/mLAtropa belladonna — 12 [hp_X]/mLGermanium sesquioxide — 12 [hp_X]/mLPotassium phosphate, Dibasic — 12 [hp_X]/mLDatura stramonium — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 6, 2016
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 43857-0398_9b9bdcb5-208c-450f-9daa-8db1746ed119SPL ID 9b9bdcb5-208c-450f-9daa-8db1746ed119SPL set ID 38905213-f20b-45d5-8e65-5f32e3839ea7UNII MA9CQJ3F7F, 00UK7646FG, 19FUJ2C58T, 7M867G6T1U, AUZ3VD75MC, 8JM482TI79, WGM46PQF02, 4GB5DQR532, 6P669D8HQ8, WQZ3G9PF0H, 96WE91N25T, CI71S98N1Z, G6W4F0V8Z3UPC 0810184340393
Pharmacologic class: Non-Standardized Food Allergenic Extract; 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

N443857039801 followed by a unit qualifier and the quantity

Package 43857-0398-01. 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 27, 2026.

Indications (excerpt from the label)

USES: For temporary relief of nervous fatigue, nervous twitch, confusion, and forgetfulness.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)