NDC 17856-1362 Rugby Nicotine Polacrilex Gum, Mint Flavor
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17856 - Atlantic Biologicals Corp.
- 17856-1362 - Rugby Nicotine Polacrilex Gum, Mint Flavor
Product Characteristics
Product Packages
NDC Code 17856-1362-1
Package Description: 50 POUCH in 1 CASE / 1 GUM, CHEWING in 1 POUCH
Product Details
What is NDC 17856-1362?
What are the uses for Rugby Nicotine Polacrilex Gum, Mint Flavor?
Which are Rugby Nicotine Polacrilex Gum, Mint Flavor UNII Codes?
The UNII codes for the active ingredients in this product are:
- NICOTINE (UNII: 6M3C89ZY6R)
- NICOTINE (UNII: 6M3C89ZY6R) (Active Moiety)
Which are Rugby Nicotine Polacrilex Gum, Mint Flavor 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:
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- MAGNESIUM OXIDE (UNII: 3A3U0GI71G)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- SODIUM CARBONATE (UNII: 45P3261C7T)
- TALC (UNII: 7SEV7J4R1U)
- XYLITOL (UNII: VCQ006KQ1E)
What is the NDC to RxNorm Crosswalk for Rugby Nicotine Polacrilex Gum, Mint Flavor?
- RxCUI: 314119 - nicotine polacrilex 2 MG Chewing Gum
- RxCUI: 314119 - nicotine 2 MG Chewing Gum
- RxCUI: 314119 - nicotine 2 MG (as nicotine polacrilex 11.1 MG) Chewing Gum
* Please review the disclaimer below.
Patient Education
Nicotine Gum
Nicotine chewing gum is used to help people stop smoking cigarettes. Nicotine chewing gum should be used together with a smoking cessation program, which may include support groups, counseling, or specific behavioral change techniques. Nicotine gum is in a class of medications called smoking cessation aids. It works by providing nicotine to your body to decrease the withdrawal symptoms experienced when smoking is stopped and as a substitute oral activity to reduce the urge to smoke.
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* 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".