Libido Pellet
NDC Package 55714-2476-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Libido (hydrastis canadensis, thuja occidentalis, agnus castus, aralia quinquefolia, baryta carbonica, berberis vulgaris, bryonia, caladium seguinum, cantharis, causticum, chelidonium majus, cinchona officinalis, conium maculatum, gaultheria procumbens, graphites, kali carbonicum, lycopodium clavatum, nux vomica, onosmodium virginianum, phosphorus, sabal serrulata, selenium metallicum, sepia, silicea, staphysagria) pellets is formulated for associated symptoms such as decreased desire, dryness, anxiety, hypersexuality and other related symptoms. This formulation utilizes a pellet delivery system. Marketed by Newton Laboratories, Inc., this product is identified by NDC 55714-2476.

Identification & Billing

NDC Package Code
55714-2476-1
Package Description
28 g in 1 BOTTLE, GLASS
Product Code
55714-2476
11-Digit Billing Format
55714247601

Clinical Specifications

Proprietary Name
Libido
Non-Proprietary Name
Hydrastis Canadensis, Thuja Occidentalis, Agnus Castus, Aralia Quinquefolia, Baryta Carbonica, Berberis Vulgaris, Bryonia, Caladium Seguinum, Cantharis, Causticum, Chelidonium Majus, Cinchona Officinalis, Conium Maculatum, Gaultheria Procumbens, Graphites, Kali Carbonicum, Lycopodium Clavatum, Nux Vomica, Onosmodium Virginianum, Phosphorus, Sabal Serrulata, Selenium Metallicum, Sepia, Silicea, Staphysagria
Substance Name
American Ginseng; Barium Carbonate; Berberis Vulgaris Root Bark; Bryonia Alba Root; Causticum; Chaste Tree Fruit; Chelidonium Majus; Cinchona Officinalis Bark; Conium Maculatum Flowering Top; Delphinium Staphisagria Seed; Dieffenbachia Seguine; Gaultheria Procumbens Top; Goldenseal; Graphite; Lycopodium Clavatum Spore; Lytta Vesicatoria; Onosmodium Virginianum; Phosphorus; Potassium Carbonate; Saw Palmetto; Selenium; Sepia Officinalis Juice; Silicon Dioxide; Strychnos Nux-vomica Seed; Thuja Occidentalis Leafy Twig
Dosage Form
Pellet - A small sterile solid mass consisting of a highly purified drug (with or without excipients) made by the formation of granules, or by compression and molding.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Formulated for associated symptoms such as decreased desire, dryness, anxiety, hypersexuality and other related symptoms.

Regulatory & Marketing

Labeler Name
Newton Laboratories, Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
01-01-2019
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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.

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 55714-2476-1 identifies a specific commercial package of 28 g in 1 bottle, glass of Libido, a human over the counter drug labeled by Newton Laboratories, Inc.. This pellet is formulated for oral use and contains american ginseng; barium carbonate; berberis vulgaris root bark; bryonia alba root; causticum; chaste tree fruit; chelidonium majus; cinchona officinalis bark; conium maculatum flowering top; delphinium staphisagria seed; dieffenbachia seguine; gaultheria procumbens top; goldenseal; graphite; lycopodium clavatum spore; lytta vesicatoria; onosmodium virginianum; phosphorus; potassium carbonate; saw palmetto; selenium; sepia officinalis juice; silicon dioxide; strychnos nux-vomica seed; thuja occidentalis 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 Newton Laboratories, Inc. on January 01, 2019. The current certification is valid through December 31, 2026.

How is this Newton Laboratories, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 55714247601. 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:

10-Digit Format (5-4-1)
55714-2476-1
11-Digit CMS (5-4-2)
55714-2476-01

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.