FDA.reportPublic FDA data

Swan 602.002/602AA

Manufacturer
Vi-Jon, LLC | Nice-Pak Products, LLC
Effective date
2026-06-24
Label type
HUMAN OTC DRUG LABEL
Version
14
Source
monthly-update
Hydrated at
2026-07-17 21:36:16

Label at a glance#

ProductEpsom Salt
Active ingredientMAGNESIUM SULFATE HEPTAHYDRATE
Label structure16 sections

Indications and uses

for relief of occasional constipation (irregularity) this product generally produces bowel movement in 1/2 to 6 hours

Dosage and administration

do not exceed recommended daily dosage drink a full glass (8 ounces) of liquie with each dose may be taken as a single daily dose or in divided doses dissolve the dose in 8 ounces of water. Lemon juice may be added to improve the taste. adults and children 12 years and over - 2 to 6 level teaspoons (10 to 30 grams) daily children 6 to under 12 years - 1 to 2 level teaspoons (5 to 10 grams) daily children under 6 y...

Label contents#

Full prescribing information#

Tamper Evident Statement

USER SAFETY WARNINGS SECTION

Tamper Evident Packaging:

Caution: This package has been sealed for your protection. Do not use if package is open, torn or mutilated.

SWAN 

Epsom Salt

MAGNESIUM SULFATE U.S.P.

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Magnesium sulfate USP (heptahydrate) 100%

Purpose

OTC - PURPOSE SECTION

Saline laxative

Uses

INDICATIONS & USAGE SECTION

  • for relief of occasional constipation (irregularity)
  • this product 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-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 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 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

  • do not exceed recommended daily dosage
  • drink a full glass (8 ounces) of liquie with each dose
  • may be taken as a single daily dose or in divided doses
  • dissolve the dose in 8 ounces of water. Lemon juice may be added to improve the taste.

adults and children 12 years and over - 2 to 6 level teaspoons (10 to 30 grams) daily

children 6 to under 12 years - 1 to 2 level teaspoons (5 to 10 grams) daily

children under 6 years - consult a doctor

Other information

SPL UNCLASSIFIED SECTION

  • each teaspoon (5 grams) contains: nagnesium 495 mg

Inactive ingredients

INACTIVE INGREDIENT SECTION

None

Side Panel

SPL UNCLASSIFIED SECTION

Saline Laxative

Magnesium Sulfate, USP

Mixes Easily, Dissolves Clear

For ages 6+

NO STIMULANTS / NON-STIMULANT ACTIVES

NO ADDED FLAVOR

NO SUGAR ADDED

PRESERVATIVE FREE

*This product generally produces bowel movement in 1/2 to 6 hours.

Adverse reaction

ADVERSE REACTIONS SECTION

Distributed by Vi-Jon, LLC

St. Louis, MO 63114

1-888-593-0593

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Cut along dotted line and press zipper to reseal.

swan ®

FAST-ACTING, EFFECTIVE RELIEF

Saline Laxative

MAGNESIUM SULFATE, USP

RELIEF IN AS FAST AS 30 MINUTES!*

Relieves Occasional Constipation and Irregularity

Meets USP Quality and Purity Standards

NET WT 1.5 LB (680.3 g)

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0869-0602-43GM - Gram0869-0602665085aa-12f6-4455-853a-5ce4bec4756212013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
MAGNESIUM SULFATE HEPTAHYDRATEACTIVE INGREDIENTSK47B8698T2
MAGNESIUM CATIONACTIVE MOIETYT6V3LHY8382

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
0869-06020869-0602-43, 0869-0602-12, 0869-0602-07, 0869-0602-45, 0869-0602-34

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
MAGNESIUM SULFATE HEPTAHYDRATESK47B8698TACTIB

Source Document#

Source XML · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
132026-03-12full-release2026-06-01 01:50:13

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
Epsom SaltMAGNESIUM SULFATEVi-Jon, LLCba490c22-19f0-4887-9509-bd3d32e0f5b12026-06-24Warnings, Adverse reactionsExact identifier
ndc (package): 0869-0602-34
ndc (package): 0869-0602-43
ndc (package): 0869-0602-12
ndc (package): 0869-0602-07
ndc (package): 0869-0602-45
ndc (product): 0869-0602
ndc11 (package): 00869060245
ndc11 (package): 00869060243
ndc11 (package): 00869060212
ndc11 (package): 00869060234
ndc11 (package): 00869060207
spl id: 55009432-e554-1075-e063-6294a90a35f8
spl set id: ba490c22-19f0-4887-9509-bd3d32e0f5b1

Reported adverse events (FAERS/openFDA)#

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