- Active ingredient
- use
-
Warnings
for this product
Ask a doctor before use if you have
- kidney disease
- a magnesium or potassium-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 pharmacist 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.
-
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 25 hours
children 2 to 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
-
principal display panel
SUNMARK
NDC 49348-504-49
DO NOT USE IF TAMPER EVIDENT TWIST-OFF CAP IS MISSING, BROKEN OR SEPARATED FROM NECKRING
Magnesium citrate
Saline Laxative
Oral Solution
Pasteurized
The sparkling laxative
Very low sodium
Alcohol Content 0.0031% (from flavoring)
CHERRY FLAVOR
Distributed by McKesson
One Post Street, San Francisco, CA 94104
Money Back Guarantee
10 FL OZ (296 mL)
-
INGREDIENTS AND APPEARANCE
MAGNESIUM CITRATE
magnesium citrate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49348-504 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) POTASSIUM BICARBONATE (UNII: HM5Z15LEBN) WATER (UNII: 059QF0KO0R) FD&C RED NO. 40 (UNII: WZB9127XOA) saccharin sodium (UNII: SB8ZUX40TY) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49348-504-49 .296 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 03/01/2002 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 03/01/2002 Labeler - McKesson (116956644) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(49348-504)