citroma

Manufacturer
Meijer Distribution, Inc | Consumer Product Partners, LLC
Effective date
2024-08-19
Label type
HUMAN OTC DRUG LABEL
Version
12
Source
legacy-cache
Hydrated at
2026-08-01 20:56:32

Label at a glance#

Productcitroma
Active ingredientMAGNESIUM CITRATE
Label structure14 sections

Dosage and administration

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 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 children under 2 years of age - ask a doctor

Label contents#

Full prescribing information#

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

for this product

Ask A Doctor

OTC - ASK DOCTOR SECTION

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

OTC - ASK DOCTOR/PHARMACIST SECTION

before use if you aretaking any other drug. Take this product 2 or more hours before or after other drugs. Laxatives may affect how other drugs work.

Stop use

OTC - STOP USE SECTION

and ask a doctor ifyou 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 help 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

  • 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 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

children under 2 years of age - ask a doctor

other information

OTHER SAFETY INFORMATION

  • each fl oz contains: magnesium 290mg
  • 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

DIST. BY MEIJER DISTRIBUTION, INC.

GRAND RAPIDS, MI 49544

www.meijer.com

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Do not use if tamper evident twist-off cap is missing, broken or separated from neckring

meijer

Lemon Flavor

Magnesium

Citrate

Oral Solution U.S.P.

Saline Laxative

Sugar Free/Low Sodium

Relief of occasional constipation

Contains no ingredient made from gluten-containing grain (wheat, barley or rye)

Alcohol content 0.012% (from flavoring)

10 FL OZ (296 mL)

image descriptionimage description

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
41250-70841250-708-38

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
3271f094-d8b9-c21a-e063-6294a90a47b158855261-1d2a-47c6-bbf1-26d4a717d7782025-04-10Warnings, Adverse reactionsExact identifier
spl set id: 58855261-1d2a-47c6-bbf1-26d4a717d778

Reported adverse events (FAERS/openFDA)#

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