NDC | 63868-944-10 |
Set ID | 35742173-74fc-47aa-942d-169272373b97 |
Category | HUMAN OTC DRUG LABEL |
Packager | QUALITY CHOICE (Chain Drug Marketing Association) |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART334 |
- Active ingredient
- 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:63868-944 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:63868-944-10 296 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 04/30/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part334 04/30/2018 Labeler - QUALITY CHOICE (Chain Drug Marketing Association) (011920774)