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  4. NDC Product Code: 68258-7991 Good Sense Nicotine

NDC 68258-7991 Good Sense Nicotine

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 68258-7991?
  5. Good Sense Nicotine Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
68258-7991
Proprietary Name:
Good Sense Nicotine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dispensing Solutions, Inc.
Labeler Code:
68258
Product Label ID:
4bb7687d-3ee0-47a3-aa43-146dede4cf55
Start Marketing Date: [9]
11-28-2009
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):
16 MM
Imprint(s):
L344
Score:
1
Flavor(s):
MINT (C73404)

Product Packages

NDC Code 68258-7991-7

Package Description: 3 VIAL in 1 CARTON / 24 LOZENGE in 1 VIAL

Product Details

What is NDC 68258-7991?

The NDC code 68258-7991 is assigned by the FDA to the product Good Sense Nicotine which is product labeled by Dispensing Solutions, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 68258-7991-7 3 vial in 1 carton / 24 lozenge in 1 vial. 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 Good Sense Nicotine?

If you are under 18 years of age, ask a doctor before usebefore using this product, read the enclosed User’s Guide for complete directions and other important informationstop smoking completely when you begin using the lozengeif you smoke your first cigarette within 30 minutes of waking up, use 4 mg nicotine lozenge if you smoke your first cigarette more than 30 minutes after waking up, use 2 mg nicotine lozenge according to the following 12 week schedule:Weeks 1 to 6Weeks 7 to 9Weeks 10 to 121 lozenge every1 to 2 hours1 lozenge every2 to 4 hours1 lozenge every4 to 8 hoursnicotine lozenge is a medicine and must be used a certain way to get the best resultsplace the lozenge in your mouth and allow the lozenge to slowly dissolve (about 20-30 minutes). Minimize swallowing. Do not chew or swallow lozenge.you may feel a warm or tingling sensationoccasionally move the lozenge from one side of your mouth to the other until completely dissolved (about 20-30 minutes)do not eat or drink 15 minutes before using or while the lozenge is in your mouthto improve your chances of quitting, use at least 9 lozenges per day for the first 6 weeksdo not use more than one lozenge at a time or continuously use one lozenge after another since this may cause you hiccups, heartburn, nausea or other side effectsdo not use more than 5 lozenges in 6 hours. Do not use more than 20 lozenges per day.stop using the nicotine lozenge at the end of 12 weeks. If you still feel the need to use nicotine lozenges, talk to your doctor.

Which are Good Sense Nicotine UNII Codes?

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

Which are Good Sense Nicotine 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:

What is the NDC to RxNorm Crosswalk for Good Sense Nicotine?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".