Magnesium Citrate

Manufacturer: H E Butt | Consumer Product Partners, LLC
Effective date: 2024-09-20
Label type: HUMAN OTC DRUG LABEL
Version: 20
Source: legacy-cache
Hydrated at: 2026-08-01 20:54:27

Label at a glance#

ProductMagnesium Citrate

Active ingredientMAGNESIUM CITRATE

Label structure14 sections

Indications and uses

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

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 divide doses adults and children 12 years of age and over - 6.5 to 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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each fl oz)

Magnesium citrate 1.745 g

purpose

OTC - PURPOSE SECTION

Saline Laxative

Uses

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
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

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 durgs work.

Stop use and ask a doctor

OTC - STOP USE SECTION

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a 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 temperature between 46° and 86°F (8° abd 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 divide doses

adults and children 12 years of age and over - 6.5 to 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

Other information

SPL UNCLASSIFIED SECTION

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

Questions

OTC - QUESTIONS SECTION

Call 1-88-593-0593

Adverse reaction

ADVERSE REACTIONS SECTION

MADE WITH PRIDE & CARE FOR H-E-B

SAN ANTONIO, TN 78204

Principal Panel Display

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

H-E-B

Magnesium Citrate

Oral solution

saline Laxative

Relief of: Occasion Constipation

Sugar & dye free

Gluten Free

Lemon Flavor

10 FL OZ (296 mL)

Do Not Use If Tamper Evident Twist-off Cap Is Missing, Broken or Separated From Neckring

image description

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
37808-769	MAGNESIUM CITRATE SOLUTION [H E BUTT]	20	Legacy NDC	20240922_91e2cf68-c61d-46d5-b9ce-c1b01fca1fcc.zip

Products#

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

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

Magnesium Citrate
BENZOIC ACID
CITRIC ACID MONOHYDRATE
EDETATE DISODIUM ANHYDROUS
SUCRALOSE
WATER
MAGNESIUM CATION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
37808-769	37808-769-38

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
BENZOIC ACID	8SKN0B0MIM	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
EDETATE DISODIUM ANHYDROUS	8NLQ36F6MM	IACT
SUCRALOSE	96K6UQ3ZD4	IACT
WATER	059QF0KO0R	IACT
MAGNESIUM CITRATE	RHO26O1T9V	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
38ccd59e-e3ec-3e9a-e063-6294a90a7f72			91e2cf68-c61d-46d5-b9ce-c1b01fca1fcc	2025-06-30	Warnings, Adverse reactions	Exact identifier spl set id: 91e2cf68-c61d-46d5-b9ce-c1b01fca1fcc

Reported adverse events (FAERS/openFDA)#

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