NDC 43772-0022 Kidney Tincture
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43772 - Synergy Formulas, Inc.
- 43772-0022 - Kidney Tincture
Product Packages
NDC Code 43772-0022-1
Package Description: 60 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43772-0022?
What are the uses for Kidney Tincture?
Which are Kidney Tincture UNII Codes?
The UNII codes for the active ingredients in this product are:
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
- PETROSELINUM CRISPUM (UNII: 1WZA4Y92EX)
- PETROSELINUM CRISPUM (UNII: 1WZA4Y92EX) (Active Moiety)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (Active Moiety)
- ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36)
- ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36) (Active Moiety)
- GLUTATHIONE (UNII: GAN16C9B8O)
- GLUTATHIONE (UNII: GAN16C9B8O) (Active Moiety)
- RUBIA TINCTORUM ROOT (UNII: 0SVP95L23G)
- RUBIA TINCTORUM ROOT (UNII: 0SVP95L23G) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- EUPATORIUM PURPUREUM ROOT (UNII: 0VYG5PVN5Q)
- EUPATORIUM PURPUREUM ROOT (UNII: 0VYG5PVN5Q) (Active Moiety)
- HYDRANGEA ARBORESCENS ROOT (UNII: SFK828Q2DE)
- HYDRANGEA ARBORESCENS ROOT (UNII: SFK828Q2DE) (Active Moiety)
- MERCURIC CHLORIDE (UNII: 53GH7MZT1R)
- MERCURIC CATION (UNII: ED30FJ8Y42) (Active Moiety)
- PORK KIDNEY (UNII: X7BCI5P86H)
- PORK KIDNEY (UNII: X7BCI5P86H) (Active Moiety)
Which are Kidney Tincture 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)
* 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".