FDA.reportPublic FDA data

Lucky Epsom Salt

Manufacturer
Delta Brands Inc
Effective date
2020-10-07
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 23:13:10

Label at a glance#

ProductLucky Epsom Salt
Active ingredientMAGNESIUM SULFATE, UNSPECIFIED FORM
Label structure13 sections

Indications and uses

■ relieves occasional constipation (irregularity) ■ generally produces bowel movement in 1/2 to 6 hours

Dosage and administration

■do not exceed more than 2 doses per day; if necessary repeat dosage in 4 hours age dose adults and children 2-4 level teaspoons dissolved 12 years and older in a full glass (8oz) of water children 6 to 1-2 level teaspoons dissolved 11 years in a full glass (8oz) of water Not recommended for children under 6 years of age

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Magnesium sulfate USP 100%

Purpose

OTC - PURPOSE SECTION

Saline laxative

Uses

INDICATIONS & USAGE SECTION

■ relieves occasional constipation (irregularity)

■ generally produces bowel movement in 1/2 to 6 hours

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

■ kidney disease ■ a magnesium restricted diet ■ stomach pain, nausea or vomiting ■ noticed a sudden change in bowel habits that lasts more than 2 weeks

Ask a doctor or pharmacist before using if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

presently taking a prescription drug

When using this product

OTC - WHEN USING SECTION

■ do not use more than directed

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ you have rectal bleeding or failure to have a bowel movement after use. This may indicate a serious condition.

■ you need to use a laxative for more than 1 week.

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 (1-800-222-1222) right away

Directions

DOSAGE & ADMINISTRATION SECTION

■do not exceed more than 2 doses per day; if necessary repeat dosage in 4 hours

age dose

adults and children 2-4 level teaspoons dissolved

12 years and older in a full glass (8oz) of water

children 6 to 1-2 level teaspoons dissolved

11 years in a full glass (8oz) of water

Not recommended for children under 6 years of age

Inactive ingredients

INACTIVE INGREDIENT SECTION

NONE

Other information

SPL UNCLASSIFIED SECTION

■ each teaspoon contains magnesium 493 mg

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct Label

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
20276-33020276-330-19, 20276-330-16, 20276-330-04, 20276-330-22

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
MAGNESIUM SULFATE, UNSPECIFIED FORMDE08037SABACTIB
MAGNESIUM CATIONT6V3LHY838IACT

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
b116ee5c-ac2b-704f-e053-2a95a90afed239bf1448-8aa1-5856-e054-00144ff88e882020-10-07WarningsExact identifier
spl id: b116ee5c-ac2b-704f-e053-2a95a90afed2
spl set id: 39bf1448-8aa1-5856-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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