NDC 63083-7007 Ret Gallbladder 7007
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63083-7007?
What are the uses for Ret Gallbladder 7007?
Which are Ret Gallbladder 7007 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ULEX EUROPAEUS FLOWER (UNII: 398DBS1PXN)
- ULEX EUROPAEUS FLOWER (UNII: 398DBS1PXN) (Active Moiety)
- ELEUTHEROCOCCUS SENTICOSUS ROOT OIL (UNII: 0DAF87OMMD)
- ELEUTHEROCOCCUS SENTICOSUS ROOT OIL (UNII: 0DAF87OMMD) (Active Moiety)
- SALIX ALBA FLOWERING TOP (UNII: XBP5X7E70R)
- SALIX ALBA FLOWERING TOP (UNII: XBP5X7E70R) (Active Moiety)
- POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632)
- POTASSIUM PHOSPHATE, UNSPECIFIED FORM (UNII: B7862WZ632) (Active Moiety)
- COPPER (UNII: 789U1901C5)
- COPPER (UNII: 789U1901C5) (Active Moiety)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- DATURA STRAMONIUM (UNII: G6W4F0V8Z3)
- DATURA STRAMONIUM (UNII: G6W4F0V8Z3) (Active Moiety)
Which are Ret Gallbladder 7007 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".