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  5. NDC Package Code: 61727-337-15 Ez-quit Control

NDC Package 61727-337-15 Ez-quit Control

Antimony Trisulfide,Dieffenbachia Seguine,Cadmium Sulfate,Strychnos Ignatii Seed,Lobelia - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
61727-337-15
Package Description:
15 mL in 1 BOTTLE, SPRAY
Product Code:
61727-337
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
Usage Information:
2 pump-sprays under the tongue, 3 times a day as needed.
11-Digit NDC Billing Format:
61727033715
Product Type:
Human Otc Drug
Labeler Name:
Homeocare Laboratories
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s):
  • Sublingual - Administration beneath the tongue.
    • Active Ingredient(s):
  • ANTIMONY TRISULFIDE 5 [hp_C]/15mL
  • CADMIUM SULFATE 5 [hp_C]/15mL
  • DIEFFENBACHIA SEGUINE 5 [hp_C]/15mL
  • LOBELIA INFLATA 5 [hp_C]/15mL
  • STRYCHNOS IGNATII SEED 5 [hp_C]/15mL
  • STRYCHNOS NUX-VOMICA SEED 5 [hp_C]/15mL
  • TOBACCO LEAF 8 [hp_C]/15mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Plant Proteins - [CS]
  • Seed Storage Proteins - [CS]
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    07-09-2012
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    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 disclaimer below.

    Frequently Asked Questions

    What is NDC 61727-337-15?

    The NDC Packaged Code 61727-337-15 is assigned to a package of 15 ml in 1 bottle, spray of Ez-quit Control, a human over the counter drug labeled by Homeocare Laboratories. The product's dosage form is spray and is administered via sublingual form.

    Is NDC 61727-337 included in the NDC Directory?

    Yes, Ez-quit Control with product code 61727-337 is active and included in the NDC Directory. The product was first marketed by Homeocare Laboratories on July 09, 2012 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 61727-337-15?

    The 11-digit format is 61727033715. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-261727-337-155-4-261727-0337-15