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Magnesium Citrate drug information

MAGNESIUM CITRATE
Chain Drug Marketing Association · ORAL

Product NDC: 83324-043

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameMAGNESIUM CITRATE
Labeler / manufacturerChain Drug Marketing Association
RouteORAL
Drug classDrug class not supplied in source label
Product NDC83324-043
Label effective date2026-08-28

Official product label reference

Magnesium Citrate — Chain Drug Marketing Association

This page contains 14 source sections for MAGNESIUM CITRATE, oral route. Label set 583b64e7-e48d-6ba6-e063-6294a90ad4d7, version 2.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Uses for relief of occasional constipation (irregularity). Generally produces bowel movement in ½ to 6 hours

Purpose

Purpose Saline laxative
Dosage and administration — label text
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 maximum 3 fl oz in 24 hours children under 2 years of age - ask a doctor
Warnings
Warnings for this product
Adverse reactions
Adverse Reactions SATISFACTION GUARANTEED 100% QC Distributed by CDMA, Inc. Nove, MI 48375 www.qualitychoice.com Questions: 800-935-2362
Active ingredient
Active ingredient (in each fl oz) Magnesium citrate 1.745 g
Ask a doctor before use
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 pharmacist
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.
When to stop use and seek help
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.
Pregnancy or breast feeding
If pregnant or breast-feeding, ask a health professional before use.
Child safety
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Storage and handling
Storage Store at temperatures between 46° and 86° F (8° and 30° C)
Unclassified section
Other information each fl oz contains: magnesium 290 mg each fl oz contains: sodium 1 mg Claims Non-USP: Non-Carbonated, Non-Pasteurized; Contains Preservatives
Inactive ingredient
Inactive ingredients benzoic acid, citric acid, disodium EDTA, flavor, sucralose, water

Official sources and product identifiers

Substances listed: MAGNESIUM CITRATE

RxNorm identifiers: 1052760

Package NDC codes

83324-043-10

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.