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  4. NDC Product Code: 10578-023 Homeopathic Stop Smoking Formula

NDC 10578-023 Homeopathic Stop Smoking Formula

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 10578-023?
  5. Homeopathic Stop Smoking Formula Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
10578-023
Proprietary Name:
Homeopathic Stop Smoking Formula
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Indiana Botanic Gardens
Labeler Code:
10578
Product Label ID:
398a1e29-e55a-4451-9ec3-20c1888c9494
Start Marketing Date: [9]
03-01-2001
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
3 MM
Imprint(s):
H;367
Score:
1

Product Packages

NDC Code 10578-023-90

Package Description: 90 TABLET in 1 BOTTLE

Product Details

What is NDC 10578-023?

The NDC code 10578-023 is assigned by the FDA to the product Homeopathic Stop Smoking Formula which is product labeled by Indiana Botanic Gardens. The product's dosage form is . The product is distributed in a single package with assigned NDC code 10578-023-90 90 tablet in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Homeopathic Stop Smoking Formula?

Helps reduce your cravings and desire for tobacco

Which are Homeopathic Stop Smoking Formula UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Homeopathic Stop Smoking Formula Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

* Please review the disclaimer below.

Product Footnotes

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

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".