NDC 58214-100 Beyond Nicotine Kit
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
GREEN (C48329)
10 MM
2
Code Structure Chart
Product Details
What is NDC 58214-100?
What are the uses for Beyond Nicotine Kit?
Which are Beyond Nicotine Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIEFFENBACHIA SEGUINE (UNII: 01800C6E6B)
- DIEFFENBACHIA SEGUINE (UNII: 01800C6E6B) (Active Moiety)
- POTASSIUM SULFATE (UNII: 1K573LC5TV)
- SULFATE ION (UNII: 7IS9N8KPMG) (Active Moiety)
- PLANTAGO MAJOR (UNII: W2469WNO6U)
- PLANTAGO MAJOR (UNII: W2469WNO6U) (Active Moiety)
- TOBACCO LEAF (UNII: 6YR2608RSU)
- TOBACCO LEAF (UNII: 6YR2608RSU) (Active Moiety)
- CALCIUM SULFATE ANHYDROUS (UNII: E934B3V59H)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
- LOBELIA INFLATA (UNII: 9PP1T3TC5U)
- LOBELIA INFLATA (UNII: 9PP1T3TC5U) (Active Moiety)
- SAMBUCUS NIGRA FLOWERING TOP (UNII: CT03BSA18U)
- SAMBUCUS NIGRA FLOWERING TOP (UNII: CT03BSA18U) (Active Moiety)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (Active Moiety)
Which are Beyond Nicotine Kit 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:
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
* 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".