NDC 68258-7992 Good Sense Nicotine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68258 - Dispensing Solutions, Inc.
- 68258-7992 - Good Sense Nicotine
Product Characteristics
Product Packages
NDC Code 68258-7992-7
Package Description: 3 VIAL in 1 CARTON / 24 LOZENGE in 1 VIAL
Product Details
What is NDC 68258-7992?
What are the uses for Good Sense Nicotine?
Which are Good Sense Nicotine UNII Codes?
The UNII codes for the active ingredients in this product are:
- NICOTINE (UNII: 6M3C89ZY6R)
- NICOTINE (UNII: 6M3C89ZY6R) (Active Moiety)
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:
- POLACRILIN (UNII: RCZ785HI7S)
- ASPARTAME (UNII: Z0H242BBR1)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MANNITOL (UNII: 3OWL53L36A)
- POTASSIUM BICARBONATE (UNII: HM5Z15LEBN)
- SODIUM ALGINATE (UNII: C269C4G2ZQ)
- SODIUM CARBONATE (UNII: 45P3261C7T)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Good Sense Nicotine?
- RxCUI: 359818 - nicotine 4 MG Oral Lozenge
- RxCUI: 359818 - nicotine 4 MG (as nicotine polacrilex 22.2 MG) Oral Lozenge
- RxCUI: 359818 - nicotine 4 MG Troche
* Please review the disclaimer below.
[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".