Label: MAGNESIUM CITRATE liquid
- NDC Code(s): 49580-0326-1
- Packager: P & L Development, LLC
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated May 18, 2023
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- Active ingredient
- Purpose
- Uses
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Warnings
Ask a doctor before use if you have
- kidney disease
- a megnesium restricted diet
- a sodium restricted diet
- stomach pain, nausea, or vomiting
- noticed a sudden change in bowel habits that lasts more than 1 week
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
- Principal Display Panel
- Package Label
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INGREDIENTS AND APPEARANCE
MAGNESIUM CITRATE
magnesium citrate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49580-0326 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MAGNESIUM CITRATE (UNII: RHO26O1T9V) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM CITRATE 1.745 g in 29.6 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) WATER (UNII: 059QF0KO0R) FD&C RED NO. 40 (UNII: WZB9127XOA) SODIUM BICARBONATE (UNII: 8MDF5V39QO) SACCHARIN SODIUM (UNII: SB8ZUX40TY) Product Characteristics Color Score Shape Size Flavor CHERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49580-0326-1 296 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/31/2015 07/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 01/31/2015 07/01/2024 Labeler - P & L Development, LLC (101896231)