Label: MAGNESIUM CITRATE liquid
- NDC Code(s): 46122-740-38
- Packager: AMERISOURCE BERGEN
- 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
- Purpose
- Uses
-
Warnings
Ask a doctor before use if you have
- Kidney disease
- a magnesium restricted diet
- Abdominal pain, nausea, or vomiting
- Noticed a sudden change in bowel habits that persists over a period of 2 weeks
- Already used a laxative for a period longer than 1 week
Ask a doctor or pharmacisy before use if you are
- Taking any other drug.
- Take this product 2 or more hours before or after other drugs. Laxatives may affect how other drugs work.
- STORAGE AND HANDLING
-
Directions
- shake well before using
- drink a full glass (8 ounces) of liquid with each dose
- may be taken as a single daily dose or in divided doses
adults and children 12 years of age and over
6.5 to 10 fl oz maximum 10 fl oz in 24 hours
children 6 to under 12 years of age
3 to 7 fl oz maximum 7 fl oz in 24 hours
children 2 to under 6 years of age
2 to 3 fl oz in 24 hours maximum 3 fl oz in 24 hours
children under 2 years of age
ask a doctor
- Other Information
- Inactive Ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
MAGNESIUM CITRATE
magnesium citrate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:46122-740 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 BENZOIC ACID (UNII: 8SKN0B0MIM) WATER (UNII: 059QF0KO0R) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SUCRALOSE (UNII: 96K6UQ3ZD4) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:46122-740-38 296 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 01/31/2023 Labeler - AMERISOURCE BERGEN (007914906) Establishment Name Address ID/FEI Business Operations Pharma Nobis, LLC 118564114 manufacture(46122-740)
