citroma

Manufacturer
NuCare Pharmaceuticals,Inc.
Effective date
2024-06-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:00:06

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 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

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 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

  • 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

OTHER SAFETY INFORMATION

  • each fl oz contains: magnesium 295 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

Distributed By McKesson

One Post Steet, San Francisco, CA 94104

Money Back Guarantee

166.00/166AA

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

pdppdp

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68071-5018-12024-06-26C16284748780-1ba0f9c33-5c04-a910-e053-dadaa90a0b85Drug Facts
68071-5018-12023-01-30C16284748780-1ba0f9c33-5c04-a910-e053-dadaa90a0b85Drug Facts
68071-5018-12021-02-19C16284748780-1ba0f9c33-5c04-a910-e053-dadaa90a0b85Drug Facts
68071-5018-12021-01-29C16284748780-1ba0f9c33-5c04-a910-e053-dadaa90a0b85Drug Facts

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70677-0051-1ML - Milliliter70677-005107e38ae9-efb1-4377-acc7-54aa3872f3ed12018-12-13

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68071-501868071-5018-1
70677-0051

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
3623347a-6f22-fd9d-e063-6394a90a2249946ce625-364b-5083-e053-2a95a90a1ebc2025-05-27Warnings, Adverse reactionsExact identifier
spl set id: 946ce625-364b-5083-e053-2a95a90a1ebc

Reported adverse events (FAERS/openFDA)#

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