NDC 0363-0015 Magnesium Citrate
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Product Details
What is NDC 0363-0015?
What are the uses for Magnesium Citrate?
Which are Magnesium Citrate UNII Codes?
The UNII codes for the active ingredients in this product are:
- MAGNESIUM CITRATE (UNII: RHO26O1T9V)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
Which are Magnesium Citrate 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)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- WINE GRAPE JUICE (UNII: JHQ6158A7R)
- WATER (UNII: 059QF0KO0R)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
What is the NDC to RxNorm Crosswalk for Magnesium Citrate?
- RxCUI: 1052760 - magnesium citrate 1.745 GM in 1 FL OZ Oral Solution
- RxCUI: 1052760 - magnesium citrate 58.2 MG/ML Oral Solution
- RxCUI: 1052760 - magnesium citrate 1.745 GM per 1 FL OZ Oral Solution
- RxCUI: 1052760 - magnesium citrate 1.745 GM per 29.6 ML Oral Solution
- RxCUI: 1052760 - magnesium citrate 1.745 GM per 30 ML Oral Solution
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Patient Education
Magnesium Citrate
Magnesium citrate is used to treat occasional constipation on a short-term basis. Magnesium citrate is in a class of medications called saline laxatives. It works by causing water to be retained with the stool. This increases the number of bowel movements and softens the stool so it is easier to pass.
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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".