NDC 63083-2007 Anti-smoking I Drops 2007
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 63083-2007?
What are the uses for Anti-smoking I Drops 2007?
Which are Anti-smoking I Drops 2007 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TOBACCO LEAF (UNII: 6YR2608RSU)
- TOBACCO LEAF (UNII: 6YR2608RSU) (Active Moiety)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- LOBELIA CARDINALIS WHOLE (UNII: GT0PJ8MB5R)
- LOBELIA CARDINALIS WHOLE (UNII: GT0PJ8MB5R) (Active Moiety)
- BEEF LUNG (UNII: 2I1RTO1MBR)
- BEEF LUNG (UNII: 2I1RTO1MBR) (Active Moiety)
- NICOTINE (UNII: 6M3C89ZY6R)
- NICOTINE (UNII: 6M3C89ZY6R) (Active Moiety)
- BETA-ENDORPHIN HUMAN (UNII: 3S51P4W3XQ)
- BETA-ENDORPHIN HUMAN (UNII: 3S51P4W3XQ) (Active Moiety)
- COFFEA ARABICA SEED, ROASTED (UNII: 9H58JRT35E)
- COFFEA ARABICA SEED, ROASTED (UNII: 9H58JRT35E) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- SUCROSE (UNII: C151H8M554)
- SUCROSE (UNII: C151H8M554) (Active Moiety)
Which are Anti-smoking I Drops 2007 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
* 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".