Adrenoplex NDC 43857-0331

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0331Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0331Add 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
43857-0331-1	43857033101	30 mL in 1 BOTTLE, DROPPER (43857-0331-1)Marketed from Nov 30, 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): Adrenoplex
Generic name (nonproprietary): chelidonium majus, echinacea (angustifolia), glandula suprarenalis bovine, spleen (suis), carduus marianus, lycopodium clavatum, natrum muriaticum, phosphoricum acidum
Active ingredients: Chelidonium majus whole — 3 [hp_X]/mLEchinacea angustifolia whole — 3 [hp_X]/mLBos taurus adrenal gland — 8 [hp_X]/mLSus scrofa spleen — 8 [hp_X]/mLMilk thistle — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLSodium chloride — 12 [hp_X]/mLPhosphoric acid — 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: Sep 2, 2014
Listing expires: Dec 31, 2026
Identifiers: Product ID 43857-0331_ead5525c-942b-48c0-8978-bcda3311b361SPL ID ead5525c-942b-48c0-8978-bcda3311b361SPL set ID 3c53c23e-7654-4e46-acf1-edb0d605ff3bUNII 7E889U5RNN, VB06AV5US8, M2776SWB29, 92AMN5J79Y, U946SH95EE, C88X29Y479, 451W47IQ8X, E4GA8884NNUPC 0210184340568

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

N443857033101 followed by a unit qualifier and the quantity

Package 43857-0331-01. 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 Dec 18, 2025.

Indications (excerpt from the label)

USES: For temporary relief of nervous exhaustion, fatigue 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)