NDC 63083-3001 Adrenal Liquescence 3001
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 63083-3001?
What are the uses for Adrenal Liquescence 3001?
Which are Adrenal Liquescence 3001 UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) (Active Moiety)
- BEE POLLEN (UNII: 3729L8MA2C)
- BEE POLLEN (UNII: 3729L8MA2C) (Active Moiety)
- PAULLINIA CUPANA SEED (UNII: C21GE7524R)
- PAULLINIA CUPANA SEED (UNII: C21GE7524R) (Active Moiety)
- ROSA CANINA FRUIT (UNII: 3TNW8D08V3)
- ROSA CANINA FRUIT (UNII: 3TNW8D08V3) (Active Moiety)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- ASIAN GINSENG (UNII: CUQ3A77YXI) (Active Moiety)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- CORTICOTROPIN (UNII: K0U68Q2TXA)
- CORTICOTROPIN (UNII: K0U68Q2TXA) (Active Moiety)
- EPHEDRA DISTACHYA FLOWERING TWIG (UNII: R55VQ87DP3)
- EPHEDRA DISTACHYA FLOWERING TWIG (UNII: R55VQ87DP3) (Active Moiety)
- ZINC (UNII: J41CSQ7QDS)
- ZINC (UNII: J41CSQ7QDS) (Active Moiety)
- EPINEPHRINE (UNII: YKH834O4BH)
- EPINEPHRINE (UNII: YKH834O4BH) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
Which are Adrenal Liquescence 3001 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".