- Active ingredient
- Use
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WARNINGS
Warnings
Ask a doctor before use if you have
- kidney disease
- a magnesium or sodium-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 a pharmacist before use if you are
taking any other drug. Take this product 2 or more more hours before or after other drugs. Laxatives may affect how other drugs work.
Stop use and ask a doctor if
you have rectal bleeding or failure to have a bowel movement after use. These could be signs of a serious condition.
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Directions
- 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 maximum 3 fl oz in 24 hours
children under 2 years of age- ask a doctor
discard unused product within 24 hours of opening bottle
- Other information
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
- principal display panel
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INGREDIENTS AND APPEARANCE
MAGNESIUM CITRATE
magnesium citrate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-666 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 CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) LEMON OIL (UNII: I9GRO824LL) POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621) water (UNII: 059QF0KO0R) SODIUM BICARBONATE (UNII: 8MDF5V39QO) SACCHARIN SODIUM (UNII: SB8ZUX40TY) SUCROSE (UNII: C151H8M554) Product Characteristics Color Score Shape Size Flavor LEMON (LEMON FLAVOR) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-666-38 .296 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 11/30/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 11/30/2017 Labeler - Target Corp (006961700) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(11673-666) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(11673-666)