Libidotone Liquid
NDC Package 44911-0741-1
Package Information
Libidotone (aralia quinquefolia, berberis vulgaris, agnus castus, avena sativa, causticum, conium maculatum, damiana, graphites, hypophysis suis, lachesis mutus, lycopodium clavatum, natrum muriaticum, phosphoricum acidum, phosphorus, selenium metallicum, sepia) liquids is adults only: 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional.If symptoms persist for more than 7 days, consult your health care professional. . This formulation utilizes a liquid delivery system. Marketed by Energique, Inc., this product is identified by NDC 44911-0741.
Identification & Billing
Clinical Specifications
- AMERICAN GINSENG 3 [hp_X]/mL
- AVENA SATIVA FLOWERING TOP 6 [hp_X]/mL
- BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL
- CAUSTICUM 12 [hp_X]/mL
- CHASTE TREE FRUIT 6 [hp_X]/mL
- CONIUM MACULATUM FLOWERING TOP 12 [hp_X]/mL
- GRAPHITE 12 [hp_X]/mL
- LACHESIS MUTA VENOM 12 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
- PHOSPHORIC ACID 12 [hp_X]/mL
- PHOSPHORUS 12 [hp_X]/mL
- SELENIUM 12 [hp_X]/mL
- SEPIA OFFICINALIS JUICE 12 [hp_X]/mL
- SODIUM CHLORIDE 12 [hp_X]/mL
- SUS SCROFA PITUITARY GLAND 12 [hp_X]/mL
- TURNERA DIFFUSA LEAFY TWIG 12 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0741 - Libidotone
- 44911-0741-1 - 30 mL in 1 BOTTLE, DISPENSING
- 44911-0741 - Libidotone
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 44911-0741-1 identifies a specific commercial package of 30 ml in 1 bottle, dispensing of Libidotone, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains american ginseng; avena sativa flowering top; berberis vulgaris root bark; causticum; chaste tree fruit; conium maculatum flowering top; graphite; lachesis muta venom; lycopodium clavatum spore; phosphoric acid; phosphorus; selenium; sepia officinalis juice; sodium chloride; sus scrofa pituitary gland; turnera diffusa leafy twig as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Energique, Inc. on February 27, 2026. The current certification is valid through December 31, 2027.
How is this Energique, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 44911074101. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.