Magnesium Citrate

Manufacturer
Medicine Shoppe International | Vi-Jon, Inc
Effective date
2020-05-12
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 23:31:06

Label at a glance#

ProductMagnesium Citrate
Active ingredientMagnesium citrate
Label structure7 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 discard unuse...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Magnesium citrate 1.745 g 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 before use if you have

OTC - ASK DOCTOR SECTION

  • kidney disease
  • a magnesium or potassium-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 a pharmacist before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

taking any other drug.  Take this product 2 or more 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 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 temperatures between 46⁰ and 86⁰ F (8⁰ and 30⁰ 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

discard unused product within 24 hours of opening bottle

Other information

OTHER SAFETY INFORMATION

  • each fl oz contains: magnesium 290 mg
  • each fl oz contains: sodium 45 mg

Ingredients

INACTIVE INGREDIENT SECTION

citric acid, lemon oil,polyethylene glycol, purified water, sodium bicarbonate, sodium saccharin, sucrose

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

The Medicine Shoppe

NDC 49614-134-42

PASTEURIZED

Magnesium Citrate

Oral Solution

SALINE LAZATIVE

LEMON FLAVOR

The Sparkling Lazative

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

100% GUARANTEED SATISFACTION

10 FL OZ (296 mL)

image descriptionimage description

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Magnesium citrateACTIVE INGREDIENTRHO26O1T9V1
magnesium cationACTIVE MOIETYT6V3LHY8381
LEMON OILINACTIVE INGREDIENTI9GRO824LL1
POTASSIUM BICARBONATEINACTIVE INGREDIENTHM5Z15LEBN1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49614-13449614-134-42

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML · Source PDF

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 12 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
LEMON OILLEMON OIL, COLD PRESSEDI9GRO824LLSUSPENSION / ORAL1 mgExact identifier — unii candidate
4 equally ranked IID candidates
LEMON OILLEMON OIL, COLD PRESSEDI9GRO824LLGEL / TOPICAL0.05 %w/wExact identifier — unii candidate
4 equally ranked IID candidates
POTASSIUM BICARBONATEPOTASSIUM BICARBONATEHM5Z15LEBNCAPSULE / ORAL174 mgExact identifier — unii candidate
8 equally ranked IID candidates
POTASSIUM BICARBONATEPOTASSIUM BICARBONATEHM5Z15LEBNSOLUTION / ORAL128 mgExact identifier — unii candidate
8 equally ranked IID candidates
POTASSIUM BICARBONATEPOTASSIUM BICARBONATEHM5Z15LEBNTABLET / BUCCAL16 mgExact identifier — unii candidate
8 equally ranked IID candidates
POTASSIUM BICARBONATEPOTASSIUM BICARBONATEHM5Z15LEBNTROCHE / ORAL60 mgExact identifier — unii candidate
8 equally ranked IID candidates
POTASSIUM BICARBONATEPOTASSIUM BICARBONATEHM5Z15LEBNLOZENGE / ORAL80 mgExact identifier — unii candidate
8 equally ranked IID candidates
LEMON OILLEMON OIL, COLD PRESSEDI9GRO824LLPASTE, DENTIFRICE / DENTAL0.7 %w/wExact identifier — unii candidate
4 equally ranked IID candidates
POTASSIUM BICARBONATEPOTASSIUM BICARBONATEHM5Z15LEBNPOWDER, FOR SOLUTION / ORAL1000 mgExact identifier — unii candidate
8 equally ranked IID candidates
POTASSIUM BICARBONATEPOTASSIUM BICARBONATEHM5Z15LEBNTABLET / SUBLINGUAL16 mgExact identifier — unii candidate
8 equally ranked IID candidates
LEMON OILLEMON OIL, COLD PRESSEDI9GRO824LLCAPSULE / ORAL8.5 mgExact identifier — unii candidate
4 equally ranked IID candidates
POTASSIUM BICARBONATEPOTASSIUM BICARBONATEHM5Z15LEBNTABLET / ORAL12.2 mgExact identifier — unii candidate
8 equally ranked IID candidates

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
ac06b7c5-8a2e-45fc-b781-d537e4a94b2c953f23ae-85e9-4e94-9597-67028bedab872021-03-25WarningsExact identifier
spl set id: 953f23ae-85e9-4e94-9597-67028bedab87

Reported adverse events (FAERS/openFDA)#

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