Appetite - Craving Control Liquid
NDC Package 55714-2386-2

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

Package Information

Appetite - Craving Control (anacardium orientale, antimon.crud., arg. nit., berber. vulg., bryonia, chelidonium majus, digitalis, graphites, humulus, iris versicolor, kali carb., lycopodium, nat. carb., nat. sulphuricum, nux vom., pulsatilla, rhus. toxicodendron, scutellaria lateriflora, sepia, stramonium, chamomilla, passiflora, valeriana.) liquids is formulated for symptoms such as overeating, cravings, fatigue, diminished appetite and emotional discomfort. This formulation utilizes a liquid delivery system. Marketed by Newton Laboratories, Inc., this product is identified by NDC 55714-2386.

Identification & Billing

NDC Package Code
55714-2386-2
Package Description
50 mL in 1 BOTTLE, GLASS
Product Code
55714-2386
11-Digit Billing Format
55714238602

Clinical Specifications

Proprietary Name
Appetite - Craving Control
Non-Proprietary Name
Anacardium Orientale, Antimon.crud., Arg. Nit., Berber. Vulg., Bryonia, Chelidonium Majus, Digitalis, Graphites, Humulus, Iris Versicolor, Kali Carb., Lycopodium, Nat. Carb., Nat. Sulphuricum, Nux Vom., Pulsatilla, Rhus. Toxicodendron, Scutellaria Lateriflora, Sepia, Stramonium, Chamomilla, Passiflora, Valeriana.
Substance Name
Antimony Trisulfide; Berberis Vulgaris Root Bark; Bryonia Alba Root; Chelidonium Majus; Datura Stramonium; Digitalis; Graphite; Hops; Iris Versicolor Root; Lycopodium Clavatum Spore; Matricaria Recutita; Passiflora Incarnata Flowering Top; Potassium Carbonate; Pulsatilla Vulgaris; Scutellaria Lateriflora; Semecarpus Anacardium Juice; Sepia Officinalis Juice; Silver Nitrate; Sodium Carbonate; Sodium Sulfate; Strychnos Nux-vomica Seed; Toxicodendron Pubescens Leaf; Valerian
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Formulated for symptoms such as overeating, cravings, fatigue, diminished appetite and emotional discomfort..

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
10-29-2018
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (55714-2386). Click a package code to view its specific billing and regulatory data.

55714-2386-0
.5 mL in 1 BOTTLE, GLASS
55714-2386-1
30 mL in 1 BOTTLE, GLASS

* 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 55714-2386-2 identifies a specific commercial package of 50 ml in 1 bottle, glass of Appetite - Craving Control, a human over the counter drug labeled by Newton Laboratories, Inc.. This liquid is formulated for oral use and contains antimony trisulfide; berberis vulgaris root bark; bryonia alba root; chelidonium majus; datura stramonium; digitalis; graphite; hops; iris versicolor root; lycopodium clavatum spore; matricaria recutita; passiflora incarnata flowering top; potassium carbonate; pulsatilla vulgaris; scutellaria lateriflora; semecarpus anacardium juice; sepia officinalis juice; silver nitrate; sodium carbonate; sodium sulfate; strychnos nux-vomica seed; toxicodendron pubescens leaf; valerian 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 October 29, 2018. 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: 55714238602. 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)
55714-2386-2
11-Digit CMS (5-4-2)
55714-2386-02

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