Magnesium Citrate

Manufacturer
Walmart Inc., | Consumer Product Partners, LLC
Effective date
2024-10-15
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
legacy-cache
Hydrated at
2026-08-01 20:52:21

Label at a glance#

ProductMagnesium Citrate
Active ingredientMAGNESIUM CITRATE
Label structure14 sections

Dosage and administration

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 in 24 hours maximum 3 fl oz in 24 hours children under 2 year...

Label contents#

Full prescribing information#

TEP

SPL UNCLASSIFIED SECTION

DO NOT USE IF TAMPER EVIDENT TWIST- OFF CAP IS MISSING, BROKEN OR SEPARATED FROM NECKRING

active ingredient

OTC - ACTIVE INGREDIENT SECTION

Magnesium citrate 1.745g per fl oz

Purpose

OTC - PURPOSE SECTION

Saline Laxative

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

Ask a doctor before use if you have

  • kidney disease
  • a magnesium restricted diet
  • abdorominal 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

OTC - ASK DOCTOR/PHARMACIST SECTION

  • 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

OTC - STOP USE SECTION

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Store at temperatures between 46° and 86°F (8° and 30° C)

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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 in 24 hours maximum 3 fl oz in 24 hours

children under 2 years of age - ask a doctor

Other information

OTHER SAFETY INFORMATION

  • each fl oz contains: magnesium 290 mg
  • each fl oz contains: sodium 1 mg

Inactive ingredients

INACTIVE INGREDIENT SECTION

benzoic acid, citric acid, disodium EDTA, flavor, sucralose, water

adverse reaction

ADVERSE REACTIONS SECTION

  Satisfaction guaranteed - For questions or comments please call 1-888-287=1915

DISTRIBUTED BY: Walmart, Inc.,

Bentonville, AR 72716

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 49035-592-38

equate

Magnesium

Citrate

Saline

Laxative

  • Relief of occasional constipation
  • For use in bowel cleansing systems for surgery or exam preparation

Grape Flavor

Empty & Replace Cap

PLASTIC

BOTTLE

how2recycle.info

Alcohol content

0.0013%

(from flavoring)

10 FL OZ (296 mL)

image descriptionimage description

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49035-592-38ML - Milliliter49035-59252ac12a4-17d7-4615-9f9e-60c2c63ac3f912023-03-13

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49035-59249035-592-38

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
33db7a63-ae3f-7087-e063-6394a90a4f30a526d804-ac60-4251-90cc-da09af4dcd1c2025-04-28Warnings, Adverse reactionsExact identifier
spl set id: a526d804-ac60-4251-90cc-da09af4dcd1c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.