Orchiforce NDC 43857-0363

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0363Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0363Add 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
43857-0363-1	43857036301	30 mL in 1 BOTTLE, DROPPER (43857-0363-1)Marketed from Apr 6, 2015

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): Orchiforce
Generic name (nonproprietary): avena sativa, damiana, agnus castus, caladium seguinum, conium maculatum, phosphoricum acidum, phosphorus, picricum acidum
Active ingredients: Avena sativa flowering top — 3 [hp_X]/mLTurnera diffusa leafy twig — 3 [hp_X]/mLChaste tree — 12 [hp_X]/mLDieffenbachia seguine — 12 [hp_X]/mLConium maculatum flowering top — 12 [hp_X]/mLPhosphoric acid — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLPicric 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: Apr 6, 2015
Listing expires: Dec 31, 2026
Identifiers: Product ID 43857-0363_da71ab12-fd57-4c1b-bfb7-ab368515d4afSPL ID da71ab12-fd57-4c1b-bfb7-ab368515d4afSPL set ID b002b03c-a772-403e-b0e8-3f75ad97208cUNII MA9CQJ3F7F, RQ2CFA7WWJ, 433OSF3U8A, 01800C6E6B, Q28R5GF371, E4GA8884NN, 27YLU75U4W, A49OS0F91S

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

N443857036301 followed by a unit qualifier and the quantity

Package 43857-0363-01. 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 Oct 17, 2024.

Indications (excerpt from the label)

INDICATIONS: For temporary relief of nervous fatigue and irresistible desires; minor nervous fatigue.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)