Label: MAGNESIUM CITRATE liquid
- NDC Code(s): 55315-327-10
- Packager: Freds Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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 January 30, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each fl oz)
- Purpose
- Uses
-
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 lasts more than 1 week
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
- Principal Display Panel
- Package Label
-
INGREDIENTS AND APPEARANCE
MAGNESIUM CITRATE
magnesium citrate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55315-327 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 GRAPE Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55315-327-10 296 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/31/2018 12/31/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 07/31/2018 12/31/2025 Labeler - Freds Inc (005866116)