NDC 58607-185 Myhephron Dialysis And Stress Supplement
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58607 - Martin Ekwealor Pharmaceu
- 58607-185 - Myhephron
Product Characteristics
Product Packages
NDC Code 58607-185-10
Package Description: 100 CAPSULE in 1 BOX
Product Details
What is NDC 58607-185?
What are the uses for Myhephron Dialysis And Stress Supplement?
Which are Myhephron Dialysis And Stress Supplement UNII Codes?
The UNII codes for the active ingredients in this product are:
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- FOLIC ACID (UNII: 935E97BOY8)
- FOLIC ACID (UNII: 935E97BOY8) (Active Moiety)
- NIACIN (UNII: 2679MF687A)
- NIACIN (UNII: 2679MF687A) (Active Moiety)
- THIAMINE (UNII: X66NSO3N35)
- THIAMINE ION (UNII: 4ABT0J945J) (Active Moiety)
- RIBOFLAVIN (UNII: TLM2976OFR)
- RIBOFLAVIN (UNII: TLM2976OFR) (Active Moiety)
- PYRIDOXINE (UNII: KV2JZ1BI6Z)
- PYRIDOXINE (UNII: KV2JZ1BI6Z) (Active Moiety)
- CYANOCOBALAMIN (UNII: P6YC3EG204)
- CYANOCOBALAMIN (UNII: P6YC3EG204) (Active Moiety)
- PANTOTHENIC ACID (UNII: 19F5HK2737)
- PANTOTHENIC ACID (UNII: 19F5HK2737) (Active Moiety)
- BIOTIN (UNII: 6SO6U10H04)
- BIOTIN (UNII: 6SO6U10H04) (Active Moiety)
Which are Myhephron Dialysis And Stress Supplement 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:
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GELATIN (UNII: 2G86QN327L)
- SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
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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".