NDC 43857-0579 Kidney Tonic II
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 43857-0579?
What are the uses for Kidney Tonic II?
Which are Kidney Tonic II UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLUTATHIONE (UNII: GAN16C9B8O)
- GLUTATHIONE (UNII: GAN16C9B8O) (Active Moiety)
- PORK KIDNEY (UNII: X7BCI5P86H)
- PORK KIDNEY (UNII: X7BCI5P86H) (Active Moiety)
- SUS SCROFA URINARY BLADDER (UNII: 3G7U72W8DA)
- SUS SCROFA URINARY BLADDER (UNII: 3G7U72W8DA) (Active Moiety)
- AGRIMONIA EUPATORIA FLOWER (UNII: 5811MI029U)
- AGRIMONIA EUPATORIA FLOWER (UNII: 5811MI029U) (Active Moiety)
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
- BRYONIA ALBA WHOLE (UNII: 56K0VVT47P)
- BRYONIA ALBA WHOLE (UNII: 56K0VVT47P) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- GALIUM APARINE WHOLE (UNII: Z4B6561488)
- GALIUM APARINE (UNII: Z4B6561488) (Active Moiety)
- RUBIA TINCTORUM ROOT (UNII: 0SVP95L23G)
- RUBIA TINCTORUM ROOT (UNII: 0SVP95L23G) (Active Moiety)
Which are Kidney Tonic II 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
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[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".