NDC 57955-0064 Artery/cholesterol/bp
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57955 - King Bio Inc.
- 57955-0064 - Artery/cholesterol/bp
Product Packages
NDC Code 57955-0064-2
Package Description: 59 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 57955-0064?
What are the uses for Artery/cholesterol/bp?
Which are Artery/cholesterol/bp UNII Codes?
The UNII codes for the active ingredients in this product are:
- GOLD (UNII: 79Y1949PYO)
- GOLD (UNII: 79Y1949PYO) (Active Moiety)
- SODIUM TETRACHLOROAURATE (UNII: 7FT6QUT299)
- TETRACHLOROAURATE ION (UNII: ZNL6IP5PJX) (Active Moiety)
- BARIUM CARBONATE (UNII: 6P669D8HQ8)
- BARIUM CATION (UNII: V645272HLN) (Active Moiety)
- BARIUM CHLORIDE DIHYDRATE (UNII: EL5GJ3U77E)
- CALCIUM FLUORIDE (UNII: O3B55K4YKI)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- CEANOTHUS AMERICANUS LEAF (UNII: 25B1Y14T8N)
- CEANOTHUS AMERICANUS LEAF (UNII: 25B1Y14T8N) (Active Moiety)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- CHOLESTEROL (UNII: 97C5T2UQ7J) (Active Moiety)
- NITROGLYCERIN (UNII: G59M7S0WS3)
- NITROGLYCERIN (UNII: G59M7S0WS3) (Active Moiety)
- LEAD IODIDE (UNII: OTL90F2GLT)
- LEAD IODIDE (UNII: OTL90F2GLT) (Active Moiety)
- STROPHANTHUS HISPIDUS SEED (UNII: MO892VI77K)
- STROPHANTHUS HISPIDUS SEED (UNII: MO892VI77K) (Active Moiety)
Which are Artery/cholesterol/bp 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)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
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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".