NDC 0536-3029 Rugby Nicotine Polacrilex Gum, Original Flavor
Nicotine Polacrilex Gum, Chewing Buccal - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0536 - Rugby Laboratories, Inc.
- 0536-3029 - Rugby Nicotine Polacrilex Gum, Original Flavor
Product Characteristics
Product Packages
NDC Code 0536-3029-06
Package Description: 5 BLISTER PACK in 1 CARTON / 10 GUM, CHEWING in 1 BLISTER PACK
Price per Unit: $0.24219 per EA
NDC Code 0536-3029-23
Package Description: 11 BLISTER PACK in 1 CARTON / 10 GUM, CHEWING in 1 BLISTER PACK
Price per Unit: $0.24219 per EA
NDC Code 0536-3029-34
Package Description: 2 BLISTER PACK in 1 CARTON / 10 GUM, CHEWING in 1 BLISTER PACK
Price per Unit: $0.24219 per EA
Product Details
What is NDC 0536-3029?
What are the uses for Rugby Nicotine Polacrilex Gum, Original Flavor?
What are Rugby Nicotine Polacrilex Gum, Original Flavor Active Ingredients?
- NICOTINE 2 mg/1 - Nicotine is highly toxic alkaloid. It is the prototypical agonist at nicotinic cholinergic receptors where it dramatically stimulates neurons and ultimately blocks synaptic transmission. Nicotine is also important medically because of its presence in tobacco smoke.
Which are Rugby Nicotine Polacrilex Gum, Original 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, Original 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:
- ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- SODIUM CARBONATE (UNII: 45P3261C7T)
- SORBITOL (UNII: 506T60A25R)
- TALC (UNII: 7SEV7J4R1U)
Which are the Pharmacologic Classes for Rugby Nicotine Polacrilex Gum, Original Flavor?
* 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.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".