Label: MAGNESIUM CITRATE SALINE LAXATIVE- magnesium citrate liquid
- NDC Code(s): 63868-943-10
- Packager: QUALITY CHOICE (Chain Drug Marketing Association)
- 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 November 30, 2020
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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.
adults and children 12 years of age and older 1/2 to 1 bottle (10 fl. oz.). Drink a full 8 oz. glass of liquid with each dose. The dose may be taken as a single daily dose or in divided doses. children 6 to 11 years of age 1/3 to 1/2 bottle with a full 8 oz. glass of liquid children under 6 years of age consult a doctor
- Other information
- Inactive ingredients
- Questions or comments?
Principal Display Panel
For Relief of Occasional Constipation
FL OZ (mL)
TAMPER EVIDENT: DO NOT USE IF THE BREAKAWAY BAND ON CAP IS BROKEN OR MISSING.
Distributed by C.D.M.A. Inc©
43157 W. Nine Mile
Novi, MI 48376-0995
- Package Label
INGREDIENTS AND APPEARANCE
MAGNESIUM CITRATE SALINE LAXATIVE
magnesium citrate liquid
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-943 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) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C RED NO. 40 (UNII: WZB9127XOA) SACCHARIN SODIUM (UNII: SB8ZUX40TY) Product Characteristics Color Score Shape Size Flavor GRAPE Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63868-943-10 296 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/31/2015 12/30/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part334 07/31/2015 12/30/2022 Labeler - QUALITY CHOICE (Chain Drug Marketing Association) (011920774)