NDC 61727-990 Freedom Quit Smoking System-nicotine Reduction Craving Control

Antimony Trisulfide, Dieffenbachia Seguine, Cadmium Sulfate, Strychnos Ignatii Seed, Lobelia Inflata, Strychnos Nux-vomica Seed, Tobacco Leaf

NDC Product Code 61727-990

NDC CODE: 61727-990

Proprietary Name: Freedom Quit Smoking System-nicotine Reduction Craving Control What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Antimony Trisulfide, Dieffenbachia Seguine, Cadmium Sulfate, Strychnos Ignatii Seed, Lobelia Inflata, Strychnos Nux-vomica Seed, Tobacco Leaf What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 61727 - Homeocare Laboratories
    • 61727-990 - Freedom Quit Smoking System-nicotine Reduction Craving Control

NDC 61727-990-30

Package Description: 30 mL in 1 BOTTLE, SPRAY

NDC Product Information

Freedom Quit Smoking System-nicotine Reduction Craving Control with NDC 61727-990 is a a human over the counter drug product labeled by Homeocare Laboratories. The generic name of Freedom Quit Smoking System-nicotine Reduction Craving Control is antimony trisulfide, dieffenbachia seguine, cadmium sulfate, strychnos ignatii seed, lobelia inflata, strychnos nux-vomica seed, tobacco leaf. The product's dosage form is spray and is administered via oral form.

Labeler Name: Homeocare Laboratories

Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Freedom Quit Smoking System-nicotine Reduction Craving Control Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ANTIMONY TRISULFIDE 5 [hp_C]/30mL
  • CADMIUM SULFATE 5 [hp_C]/30mL
  • STRYCHNOS IGNATII SEED 5 [hp_C]/30mL
  • LOBELIA INFLATA 5 [hp_C]/30mL
  • STRYCHNOS NUX-VOMICA SEED 5 [hp_C]/30mL
  • TOBACCO LEAF 9 [hp_C]/30mL
  • DIEFFENBACHIA SEGUINE 5 [hp_C]/30mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Homeocare Laboratories
Labeler Code: 61727
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 09-14-2012 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Freedom Quit Smoking System-nicotine Reduction Craving Control Product Label Images

Freedom Quit Smoking System-nicotine Reduction Craving Control Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Antimonium crudum 5C, Caladium seg. 6C, Cadmium sulph 5C, Ignatia amara 5C, Lobelia inflata 5C, Nux vomica 5C (Poison nut), Tabacum (Tobacco) 5C, 7C, 9C.

Inactive Ingredients:

Purified water, Ethyl alcohol 20%.

Warnings:

If you are pregnant or nursing, or if you have a serious condition, seek the advice of a doctor before using this product.

Keep Out Of Reach Of Children.

Keep out of reach of children.

Purpose:

Temporarily relieves cravings for cigarettes & tobacco.

Indications And Usage:

2 pump-sprays under the tongue, 3 times a day or as needed.

Dosage And Administration:

2 pump-sprays under the tongue, 3 times a day or as needed.

Freedom Quit Smoking System-Nicotine Reduction Craving Control Spray

FREEDOM Quit Smoking System-Nicotine Reduction Craving Control SprayNicotine FreeHomeopathic Medicine60 sprays (10 day supply)HCL-Freedom-Quit-Smoking-System.jpg

* Please review the disclaimer below.