Label: MAGNESIUM CITRATE liquid
- NDC Code(s): 55315-009-10
- Packager: Freds Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 28, 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
- amagnesium 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
- 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:55315-009 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:55315-009-10 296 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 03/31/2018 06/30/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 03/31/2018 06/30/2024 Labeler - Freds Inc (005866116)