Male Balance NDC 44911-0613

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0613Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0613Add 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
44911-0613-1	44911061301	30 mL in 1 BOTTLE, DROPPER (44911-0613-1)Marketed from May 25, 2021

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): Male Balance
Generic name (nonproprietary): avena sativa, hepar suis, orchitinum (suis), testosterone, agnus castus, damiana, ginkgo biloba, hypothalamus (suis), lycopodium clabatum, human growth hormone, epimedium grandiflorum, serotonin (hydrochloride)
Active ingredients: Avena sativa flowering top — 6 [hp_X]/mLPork liver — 6 [hp_X]/mLSus scrofa testicle — 6 [hp_X]/mLTestosterone — 6 [hp_X]/mLChaste tree fruit — 12 [hp_X]/mLTurnera diffusa leafy twig — 12 [hp_X]/mLGinkgo — 12 [hp_X]/mLSus scrofa hypothalamus — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLSomatropin — 26 [hp_X]/mLEpimedium grandiflorum top — 30 [hp_X]/mLSerotonin hydrochloride — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique,Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 25, 2021
Listing expires: Dec 31, 2026
DEA schedule: CIII
Other FDA classes: Androgen Receptor Agonists (Mechanism)Androstanes (Chemical structure)Human Growth Hormone (Chemical structure)
Identifiers: Product ID 44911-0613_6b4ae3c0-cbfb-40cf-965f-e4bd2b961a2dSPL ID 6b4ae3c0-cbfb-40cf-965f-e4bd2b961a2dSPL set ID 297fe55b-ac23-4a7f-bbbe-1005c0066931UNII MA9CQJ3F7F, 6EC706HI7F, KM02613O28, 3XMK78S47O, 433OSF3U8A, RQ2CFA7WWJ, 19FUJ2C58T, N6R0856Z79, C88X29Y479, NQX9KB6PCL, 137PC46F89, GKN429M9VS
Pharmacologic class: Androgen; Recombinant Human Growth Hormone

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

N444911061301 followed by a unit qualifier and the quantity

Package 44911-0613-01. 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 26, 2024.

Indications (excerpt from the label)

INDICATIONS: 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)