What is NDC 44911-0552?

44911-0552 is the product NDC for Erogetone, American ginseng 3 [hp_X]/mL + 10 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Erogetone (Aralia Quinquefolia, Berberis Vulgaris, Causticum, Conium Maculatum, Damiana, Graphites, Lachesis Mutus, Natrum Muriaticum, Phosphoricum Acidum, Phosphorus, Sepia).

What is the active ingredient?

American ginseng, Berberis vulgaris root bark, Causticum, Conium maculatum flowering top, Turnera diffusa leafy twig, Graphite, Lachesis muta venom, Sodium chloride, Phosphoric acid, Phosphorus, Sepia officinalis juice.

Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Erogetone?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Erogetone NDC 44911-0552 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0552Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0552Add 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
44911-0552-1	4491105520144911055201	30 mL in 1 BOTTLE, DROPPER (44911-0552-1)Marketed from Oct 6, 2020

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): Erogetone
Generic name (nonproprietary): aralia quinquefolia, berberis vulgaris, causticum, conium maculatum, damiana, graphites, lachesis mutus, natrum muriaticum, phosphoricum acidum, phosphorus, sepia
Active ingredients: American ginseng — 3 [hp_X]/mLBerberis vulgaris root bark — 3 [hp_X]/mLCausticum — 12 [hp_X]/mLConium maculatum flowering top — 12 [hp_X]/mLTurnera diffusa leafy twig — 12 [hp_X]/mLGraphite — 12 [hp_X]/mLLachesis muta venom — 12 [hp_X]/mLSodium chloride — 12 [hp_X]/mLPhosphoric acid — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLSepia officinalis juice — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.NDC labeler code 44911
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 6, 2020
Marketing end: Oct 26, 2026
Identifiers: Product ID 44911-0552_ac359f38-feb3-49b4-b9b0-6a291ec67aa6SPL ID ac359f38-feb3-49b4-b9b0-6a291ec67aa6SPL set ID 1e872ecd-e7a5-463d-9832-47b7046096dbUNII 8W75VCV53Q, 1TH8Q20J0U, DD5FO1WKFU, Q28R5GF371, RQ2CFA7WWJ, 4QQN74LH4O, VSW71SS07I, 451W47IQ8X, E4GA8884NN, 27YLU75U4W, QDL83WN8C2UPC 0363113700695

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

N444911055201 followed by a unit qualifier and the quantity

Package 44911-0552-01. 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 Jun 28, 2022.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve symptoms in women such as decreased sexal desire and feelings of fatigue.** **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)

About NDC 44911-0552

What is NDC 44911-0552?: 44911-0552 is the product NDC for Erogetone, American ginseng 3 [hp_X]/mL + 10 more ingredients liquid, listed with the FDA by Energique, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Erogetone (Aralia Quinquefolia, Berberis Vulgaris, Causticum, Conium Maculatum, Damiana, Graphites, Lachesis Mutus, Natrum Muriaticum, Phosphoricum Acidum, Phosphorus, Sepia).
What is the active ingredient?: American ginseng, Berberis vulgaris root bark, Causticum, Conium maculatum flowering top, Turnera diffusa leafy twig, Graphite, Lachesis muta venom, Sodium chloride, Phosphoric acid, Phosphorus, Sepia officinalis juice.
Who is the labeler?: Energique, Inc., NDC labeler code 44911. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Erogetone?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.