Natural Testosterone NDC 43857-0268

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0268Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0268Add 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
43857-0268-1	43857026801	30 mL in 1 BOTTLE, SPRAY (43857-0268-1)Marketed from May 4, 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): Natural Testosterone
Generic name (nonproprietary): avena sativa. epimedium, lycopodium clavatum, damiana, testosterone, agnus castus
Active ingredients: Avena sativa flowering top — 3 [hp_X]/mLEpimedium grandiflorum top — 3 [hp_X]/mLLycopodium clavatum spore — 3 [hp_X]/mLTurnera diffusa leafy twig — 6 [hp_X]/mLTestosterone — 8 [hp_X]/mLChaste tree — 12 [hp_X]/mL
Dosage form: Spray
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 24, 2014
Listing expires: Dec 31, 2027
DEA schedule: CIII
Other FDA classes: Androgen Receptor Agonists (Mechanism)Androstanes (Chemical structure)
Identifiers: Product ID 43857-0268_09655bdc-c2fe-49cf-9132-1060615e0303SPL ID 09655bdc-c2fe-49cf-9132-1060615e0303SPL set ID e2e6ce46-6729-4a63-90db-27e933379f45UNII MA9CQJ3F7F, 137PC46F89, C88X29Y479, RQ2CFA7WWJ, 3XMK78S47O, 433OSF3U8AUPC 0810184340300
Pharmacologic class: Androgen

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

N443857026801 followed by a unit qualifier and the quantity

Package 43857-0268-01. 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 17, 2026.

Indications (excerpt from the label)

USES: For temporary relief of sexual debility from nervous prostration, for enhancing sexual function, nervous exhaustion causing lack of sexual desire.** **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)