NDC 57955-0277 M3 Metabolic Mineral Modulator
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57955 - King Bio Inc.
- 57955-0277 - M3 Metabolic Mineral Modulator
Product Packages
NDC Code 57955-0277-2
Package Description: 59 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 57955-0277?
What are the uses for M3 Metabolic Mineral Modulator?
Which are M3 Metabolic Mineral Modulator UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- CALCIUM FLUORIDE (UNII: O3B55K4YKI)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
- GUAIAC (UNII: 03C8A0DFJ8)
- GUAIAC (UNII: 03C8A0DFJ8) (Active Moiety)
- HEKLA LAVA (UNII: C21158IIRK)
- HEKLA LAVA (UNII: C21158IIRK) (Active Moiety)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV) (Active Moiety)
- PARATHYROID HORMONE (UNII: N19A0T0E5J)
- PARATHYROID HORMONE (UNII: N19A0T0E5J) (Active Moiety)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- PYRIDOXINE (UNII: KV2JZ1BI6Z) (Active Moiety)
Which are M3 Metabolic Mineral Modulator 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)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
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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".