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  4. NDC Product Code: 53852-0002 Smoke Remedy

NDC 53852-0002 Smoke Remedy

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 53852-0002?
  4. Smoke Remedy Uses
  5. Active Ingredients UNII Codes
  6. 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:
53852-0002
Proprietary Name:
Smoke Remedy
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Living Well Remedies, Llc
Labeler Code:
53852
Product Label ID:
f20534e5-0e0a-4407-806f-9282db64b5c6
Start Marketing Date: [9]
02-10-2011
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 53852-0002-4

Package Description: 118 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 53852-0002?

The NDC code 53852-0002 is assigned by the FDA to the product Smoke Remedy which is product labeled by Living Well Remedies, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 53852-0002-4 118 ml in 1 bottle, spray . 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 Smoke Remedy?

Uses:Can help to stop smoking by reducing the craving and desire for tobacco smoke or chew. Helps prevent irritability, anxiety, nervousness and difficulty sleeping when quitting.

Which are Smoke Remedy UNII Codes?

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

Which are Smoke Remedy 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:

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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".