Ez-quit Control Spray
NDC Package 61727-337-15

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

Package Information

Ez-quit Control (antimony trisulfide, dieffenbachia seguine, cadmium sulfate, strychnos ignatii seed, lobelia inflata, strychnos nux-vomica seed, tobacco leaf) sprays is 2 pump-sprays under the tongue, 3 times a day as needed. This formulation utilizes a spray delivery system. Marketed by Homeocare Laboratories, this product is identified by NDC 61727-337.

Identification & Billing

NDC Package Code
61727-337-15
Package Description
15 mL in 1 BOTTLE, SPRAY
Product Code
61727-337
11-Digit Billing Format
61727033715

Clinical Specifications

Proprietary Name
Ez-quit Control
Non-Proprietary Name
Antimony Trisulfide, Dieffenbachia Seguine, Cadmium Sulfate, Strychnos Ignatii Seed, Lobelia Inflata, Strychnos Nux-vomica Seed, Tobacco Leaf
Substance Name
Antimony Trisulfide; Cadmium Sulfate; Dieffenbachia Seguine; Lobelia Inflata; Strychnos Ignatii Seed; Strychnos Nux-vomica Seed; Tobacco Leaf
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route
Sublingual - Administration beneath the tongue.
Active Ingredient(s)
Pharmacologic Class
Usage Information
2 pump-sprays under the tongue, 3 times a day as needed.

Regulatory & Marketing

Labeler Name
Homeocare Laboratories
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
07-09-2012
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 61727-337-15 identifies a specific commercial package of 15 ml in 1 bottle, spray of Ez-quit Control, a human over the counter drug labeled by Homeocare Laboratories. This spray is formulated for sublingual use and contains antimony trisulfide; cadmium sulfate; dieffenbachia seguine; lobelia inflata; strychnos ignatii seed; strychnos nux-vomica seed; tobacco leaf 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 Homeocare Laboratories on July 09, 2012. The current certification is valid through December 31, 2026.

How is this Homeocare Laboratories product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 61727033715. 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 (5-3-2)
61727-337-15
11-Digit CMS (5-4-2)
61727-0337-15

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