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Magnesium Citrate by NuCare Pharmaceuticals,Inc.

Dosage form: liquid
Ingredients: MAGNESIUM CITRATE 1.745g in 29.6mL
Labeler: NuCare Pharmaceuticals,Inc.
NDC Code: 68071-4128

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.

Sunmark Magnesium Citrate

Active ingredient
Magnesium citrate 1.745 g per fl oz

Saline laxative

Use for relief of occasional constipation (irregularity).  Generally produces bowel movement in 1/2 to 6 hours


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.

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.

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

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
•magnesium content 290 mg per 1 fl oz (30 mL)
•potassium content 80 mg per 1 fl oz (30 mL)
•store at temperaturs between 46⁰ and 86⁰ F (8⁰ and 30⁰ C)

Inactive ingredients cherry flavor, citric acid, FD+C red # 40, potassium bicarbonate, sodium saccharin, water purified

magnesium citrate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68071-4128(NDC:49348-504)
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
FD&C RED NO. 40 
#Item CodePackage Description
1NDC:68071-4128-10.296 mL in 1 BOTTLE, GLASS
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33403/01/2002
Labeler - NuCare Pharmaceuticals,Inc. (010632300)
NuCare Pharmaceuticals,Inc.010632300relabel(68071-4128)

NuCare Pharmaceuticals,Inc.

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Medically reviewed on Oct 25, 2017

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.