Label: MAGNESIUM CITRATE liquid
- NDC Code(s): 56062-329-10
- Packager: Publix Supermarkets, Inc.
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated April 27, 2023
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
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Warnings
Ask a doctor before use if you have
- kidney disease
- a magnesium restricted diet
- a sodium restricted diet
- stomach pain, nausea, or vomiting
- noticed a sudden change in bowel habits that last more than 1 week
- Directions
- Other information
- Inactive ingredients
- 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:56062-329 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) SODIUM BICARBONATE (UNII: 8MDF5V39QO) WATER (UNII: 059QF0KO0R) SACCHARIN SODIUM ANHYDROUS (UNII: I4807BK602) Product Characteristics Color Score Shape Size Flavor LEMON Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:56062-329-10 296 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/28/2019 02/28/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 02/28/2019 02/28/2024 Labeler - Publix Supermarkets, Inc. (006922009)