DHEA Forte NDC 43857-0052

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0052Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0052Add 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
43857-0052-1	43857005201	30 mL in 1 BOTTLE, SPRAY (43857-0052-1)Marketed from Mar 15, 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): DHEA Forte
Generic name (nonproprietary): dehydroepiandrosterone (dhea), pregnenolone, progesterone,
Active ingredients: Prasterone — 6 [hp_X]/mLPregnenolone — 6 [hp_X]/mLProgesterone — 6 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritionals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 7, 2012
Listing expires: Dec 31, 2027
Other FDA classes: Progesterone (Chemical structure)
Identifiers: Product ID 43857-0052_b7e4c39c-d2eb-49f4-8411-63a44fe87684SPL ID b7e4c39c-d2eb-49f4-8411-63a44fe87684SPL set ID 663affc1-0998-4231-b284-ff3e2a7807b9UNII 459AG36T1B, 73R90F7MQ8, 4G7DS2Q64Y
Pharmacologic class: Progesterone

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

N443857005201 followed by a unit qualifier and the quantity

Package 43857-0052-01. 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 Apr 3, 2026.

Indications (excerpt from the label)

USES: For temporary relief of stressful situations, lowered immune response, inflammation processes, enhances calcium metabolism in bones, improves moods, and enhances cell metabolism.** **Claims based on traditional homeopathic practices, 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)