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Manufacturer: Geri-Care Pharmaceuticals, Corp
Effective date: 2026-05-28
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: daily-update
Hydrated at: 2026-06-12 05:10:12

Label at a glance#

ProductMagnesium Citrate

Active ingredientMAGNESIUM CITRATE

Label structure9 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 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 ...

Contacts and useful links#

PhoneLabel contact1-800-540-3765

Label contents#

Full prescribing information#

Active ingredient (in each fl oz)

OTC - ACTIVE INGREDIENT SECTION

Magnesium citrate 1.745g

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

Warnings

Do not use

OTC - DO NOT USE SECTION

laxative products for longer than 1 week unless directed by a doctor.

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

kidney disease
a magnesium restricted diet
a sodium restricted diet
abdominal pain, nausea, or vomiting
noticed a sudden change in bowel habits that persists over a period of 2 weeks

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 bowel movement after use. These could be signs of a serious condition.

If pregnant or breast-feeding,

PREGNANCY 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.

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, 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, sodium 1 mg
store at 46-86ºF (8-30ºC)
do not refrigerate
protect from excessive heat and freezing

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Questions?

OTC - QUESTIONS SECTION

1-800-540-3765

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0357896266103	GTIN-13: 0357896266103 EAN-13: 0357896266103 GTIN-12: 357896266103 UPC-A: 357896266103 GTIN storage (14 digits): 00357896266103	qcom.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
57896-266-10	2021-02-15	C162847	48780-1	ba0f9c33-16ec-a910-e053-dadaa90a0b85	qcom
57896-266-10	2021-01-29	C162847	48780-1	ba0f9c33-16ec-a910-e053-dadaa90a0b85	qcom

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
57896-266-10	ML - Milliliter	57896-266	04101550-1dd1-42c8-83e0-5a0c0212dd2d	1	2020-03-10

Products#

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

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
57896-266	57896-266-10

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

Source Document#

Source XML · Source PDF

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
Magnesium Citrate	MAGNESIUM CITRATE	Geri-Care Pharmaceuticals, Corp	99eb67ca-301c-dfdb-e053-2a95a90aff6f	2026-05-28	Warnings	Exact identifier ndc (package): 57896-266-10 ndc (product): 57896-266 ndc11 (package): 57896026610 spl id: 52e2f2b8-b4f4-354a-e063-6294a90a076e spl set id: 99eb67ca-301c-dfdb-e053-2a95a90aff6f

Reported adverse events (FAERS/openFDA)#

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