Warming Epsom Rub

Manufacturer
OLD EAST MAIN CO
Effective date
2023-02-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:36:03

Label at a glance#

ProductWarming Epsom Rub
Active ingredientMENTHOL
Label structure14 sections

Dosage and administration

adults and children 2 years of age and older  - apply to affected area not more than 3 to 4 times daily children under 2 years of age - consult a doctor Directions for Use as Relaxing Soak Solution: For external use only.  Pour Liberally into warm water no more than 4 times daily

Label contents#

Full prescribing information#

active ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol (1.25 w/w)

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Use

INDICATIONS & USAGE SECTION

for the temporry relief of minor aches and pains of muscle joints associated with simple backache, arthritis, strains, bruises, and sprains

Warnings

WARNINGS SECTION

For external use only

Flammable

SPL UNCLASSIFIED SECTION

  • keep away from fire or flame, heat, spark, electrical

When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes
  • do not apply to wounds or damaged skin
  • do not bandage tightly

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worsens, or if symptoms persist for more then 7 days or clear up and occur again within a few days

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right way.

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children 2 years of age and older  - apply to affected area not more than 3 to 4 times daily

children under 2 years of age - consult a doctor

Directions for Use as Relaxing Soak Solution:

For external use only.  Pour Liberally into warm water no more than 4 times daily

Caution

SPL UNCLASSIFIED SECTION

If prompt relief is not obtained or there is evidence of infection, discontinue use and consult your physician.  Individuals with diabetes should not use for hot or warm soaks unless advised by a physician.

Other information

SPL UNCLASSIFIED SECTION

  • does not contain, nor is intended as a substitute for grain or ethyl alcohol
  • will produce serious gastric distributances if taken internally
  • fumes can be acutely irritating to respiratory system.  Avoid inhaling this product

inactive ingredients

INACTIVE INGREDIENT SECTION

water, isopropyl alcohol, Capsicum frutescens fruit extract, methyl salicylate, magnesium sulfate, red 40

SPL UNCLASSIFIED SECTION

FOR EXTERNAL USE AS A SOAK: POUR LIBERALLY INTO WARM WATER NO MORE THAN 4 TIMES DAILY.

CAUTION: IF PROMPT RELIEF IS NOT OBTAINED OR THERE IS EVIDENCE OF INFECTION, DISCONTINUE USE AND CONSULT YOUR PHYSICIAN. HOT OR WARM SOAKS SHOULD NOT BE USED BY INDIVIDUALS WITH DIABETES EXCEPT ON THE ADVICE OF A PHYSICIAN. KEEP OUT OF REACH OF CHILDREN.

DISTRIBUTED BY OLD EAST MAIN

100 MISSION RIDGE

GOODLETTSVILLE, TN 37072

672.000/672AA

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Rexall

Permeating Heat Sports Rub

PAIN RELIEVING & SOAKING SOLUTION

Penetrating pain relief

Temporarily relieves pains associated with:

  • Arthritis
  • Minor aches
  • Sprains
  • Tired feet

16 FL OZ (1 PT) 473 mL

image descriptionimage description

Products#

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55910-67255910-672-43

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
2424173d-cc57-d778-e063-6394a90ab6a8696b4a7e-28b4-4f87-b8db-17649ac42cef2024-10-10WarningsExact identifier
spl set id: 696b4a7e-28b4-4f87-b8db-17649ac42cef

Reported adverse events (FAERS/openFDA)#

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