NDC 50181-0021 Mbm 4 Kidney
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50181 - The Wellness Center
- 50181-0021 - Mbm 4 Kidney
Product Packages
NDC Code 50181-0021-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 50181-0021?
What are the uses for Mbm 4 Kidney?
Which are Mbm 4 Kidney UNII Codes?
The UNII codes for the active ingredients in this product are:
- PORK KIDNEY (UNII: X7BCI5P86H)
- PORK KIDNEY (UNII: X7BCI5P86H) (Active Moiety)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50)
- SOLIDAGO VIRGAUREA FLOWERING TOP (UNII: 5405K23S50) (Active Moiety)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
- BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
- HUMAN BREAST TUMOR CELL (UNII: C62OO7VD9K)
- HUMAN BREAST TUMOR CELL (UNII: C62OO7VD9K) (Active Moiety)
- ATROPA BELLADONNA WHOLE (UNII: DSV74G1P2J)
- ATROPA BELLADONNA WHOLE (UNII: DSV74G1P2J) (Active Moiety)
- CICUTA VIROSA ROOT (UNII: YEA9P21S8N)
- CICUTA VIROSA ROOT (UNII: YEA9P21S8N) (Active Moiety)
- NITRIC ACID (UNII: 411VRN1TV4)
- NITRIC ACID (UNII: 411VRN1TV4) (Active Moiety)
- ACONITUM NAPELLUS (UNII: U0NQ8555JD)
- ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
- SILVER NITRATE (UNII: 95IT3W8JZE)
- SILVER CATION (UNII: 57N7B0K90A) (Active Moiety)
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
Which are Mbm 4 Kidney 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".