NDC 63083-7008 Ret Liver 7008
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 63083-7008?
What are the uses for Ret Liver 7008?
Which are Ret Liver 7008 UNII Codes?
The UNII codes for the active ingredients in this product are:
- CICHORIUM INTYBUS FLOWER (UNII: HW54500A89)
- CICHORIUM INTYBUS FLOWER (UNII: HW54500A89) (Active Moiety)
- VERBENA OFFICINALIS FLOWERING TOP (UNII: 311PNK9CDZ)
- VERBENA OFFICINALIS FLOWERING TOP (UNII: 311PNK9CDZ) (Active Moiety)
- SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE (UNII: 70WT22SF4B)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD)
- ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD) (Active Moiety)
- ANACARDIUM OCCIDENTALE BARK (UNII: 02I3VKA20E)
- ANACARDIUM OCCIDENTALE BARK (UNII: 02I3VKA20E) (Active Moiety)
- GOLD (UNII: 79Y1949PYO)
- GOLD (UNII: 79Y1949PYO) (Active Moiety)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
- POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
- NITRIC ACID (UNII: 411VRN1TV4)
- NITRIC ACID (UNII: 411VRN1TV4) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV)
- DELPHINIUM STAPHISAGRIA SEED (UNII: 00543AP1JV) (Active Moiety)
Which are Ret Liver 7008 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".