MAGNESIUM CITRATE- magnesium citrate liquid 
NuCare Pharmaceuticals,Inc.

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.

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Sunmark Magnesium Citrate

Active ingredient
Magnesium citrate 1.745 g per fl oz

Purpose
Saline laxative

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

Warnings

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

pdp

MAGNESIUM CITRATE 
magnesium citrate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68071-4128(NDC:49348-504)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MAGNESIUM CITRATE (UNII: RHO26O1T9V) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM CITRATE1.745 g  in 29.6 mL
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
POTASSIUM BICARBONATE (UNII: HM5Z15LEBN)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68071-4128-10.296 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product10/25/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33403/01/2002
Labeler - NuCare Pharmaceuticals,Inc. (010632300)
Establishment
NameAddressID/FEIBusiness Operations
NuCare Pharmaceuticals,Inc.010632300relabel(68071-4128)

Revised: 2/2022
Document Id: d7765fc5-3592-1e75-e053-2a95a90a5fbf
Set id: 5c664215-758d-a7a8-e053-2a91aa0a570e
Version: 4
Effective Time: 20220207
 
NuCare Pharmaceuticals,Inc.