Label: MAGNESIUM CITRATE SALINE LAXATIVE- magnesium citrate liquid
- NDC Code(s): 56062-326-10
- 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.
Updated March 21, 2019
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- Active ingredient
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
Stop use and ask a doctor if
you have rectal bleeding or no bowel movement after use. These could be signs of a serious condition.
- Other information
- Inactive ingredients
- Principal Display Panel
- Package Label
INGREDIENTS AND APPEARANCE
MAGNESIUM CITRATE SALINE LAXATIVE
magnesium citrate liquid
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:56062-326 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) SACCHARIN SODIUM (UNII: SB8ZUX40TY) FD&C RED NO. 40 (UNII: WZB9127XOA) SODIUM BICARBONATE (UNII: 8MDF5V39QO) Product Characteristics Color Score Shape Size Flavor CHERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:56062-326-10 296 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 02/28/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part334 02/28/2019 Labeler - Publix Supermarkets, Inc. (006922009)