Vital Female Sexual Energy Spray
NDC Package 50845-0261-2
Package Information
Vital Female Sexual Energy (agnus castus, arnica montana, avena sativa, caulophyllum thalictroides, cinchona officinalis, damiana, hypophysis suis, l-arginine, natrum muriaticum, onosmodium virginianum, oophorinum suis, phosphoricum acidum, sepia, thuja occidentalis) sprays is adults only. Spray twice under the tongue three times a day. This formulation utilizes a spray delivery system. Marketed by Liddell Laboratories, Inc., this product is identified by NDC 50845-0261.
Identification & Billing
Clinical Specifications
- ARGININE 6 [hp_X]/mL
- ARNICA MONTANA WHOLE 3 [hp_X]/mL
- AVENA SATIVA FLOWERING TOP 3 [hp_X]/mL
- CAULOPHYLLUM THALICTROIDES ROOT 6 [hp_X]/mL
- CHASTE TREE FRUIT 3 [hp_X]/mL
- CINCHONA OFFICINALIS BARK 3 [hp_X]/mL
- ONOSMODIUM VIRGINIANUM 30 [hp_C]/mL
- PHOSPHORIC ACID 200 [hp_C]/mL
- SEPIA OFFICINALIS JUICE 30 [hp_C]/mL
- SODIUM CHLORIDE 6 [hp_X]/mL
- SUS SCROFA OVARY 30 [hp_C]/mL
- SUS SCROFA PITUITARY GLAND 12 [hp_X]/mL
- THUJA OCCIDENTALIS LEAFY TWIG 30 [hp_C]/mL
- TURNERA DIFFUSA LEAFY TWIG 1 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 50845 - Liddell Laboratories, Inc.
- 50845-0261 - Vital Female Sexual Energy
- 50845-0261-2 - 1 BOTTLE, SPRAY in 1 CARTON / 30 mL in 1 BOTTLE, SPRAY (50845-0261-1)
- 50845-0261 - Vital Female Sexual Energy
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 50845-0261-2 identifies a specific commercial package of 1 bottle, spray in 1 carton / 30 ml in 1 bottle, spray (50845-0261-1) of Vital Female Sexual Energy, a human over the counter drug labeled by Liddell Laboratories, Inc.. This spray is formulated for oral use and contains arginine; arnica montana whole; avena sativa flowering top; caulophyllum thalictroides root; chaste tree fruit; cinchona officinalis bark; onosmodium virginianum; phosphoric acid; sepia officinalis juice; sodium chloride; sus scrofa ovary; sus scrofa pituitary gland; thuja occidentalis leafy twig; 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 Liddell Laboratories, Inc. on March 25, 2020.
How is this Liddell Laboratories, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 50845026102. 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.