FOOT SOAK

Manufacturer: Xtreme Tools International, Inc
Effective date: 2024-12-28
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 20:43:56

Label at a glance#

ProductFOOT SOAK

Active ingredientMETHYL SALICYLATE, MENTHOL

Label structure11 sections

Dosage and administration

Pour a desired amount of Foot Soak into pan or tub of warm water. Soak for as long as desired.

Contacts and useful links#

PhoneLabel contact1-305-622-7474

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 5%

Methyl Salicylate 5%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Use

INDICATIONS & USAGE SECTION

For the Temporary relief of minor pain.

Warning

WARNINGS SECTION

For External use only.

If pregnant or breast-feeding, ask a health professional before use.

Allergy Alert:
If prone to allergic reaction from aspirin or salicylate, consult a doctor before use.

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Condition worsens or does not improve after regular use of this product.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Pour a desired amount of Foot Soak into pan or tub of warm water. Soak for as long as desired.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Sodium Chloride (Himalayan Pink Salt)

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-305-622-7474 Monday through Friday 9:00 AM to 5:00 PM

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1133 gr in JAR; NDC 74553-005-01

foot Soak

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

FOOT SOAK
Menthol, Methyl Salicylate
METHYL SALICYLATE
SALICYLIC ACID
MENTHOL
SODIUM CHLORIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74553-005	74553-005-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
METHYL SALICYLATE	LAV5U5022Y	ACTIB
MENTHOL	L7T10EIP3A	ACTIB
SODIUM CHLORIDE	451W47IQ8X	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
b6937a24-2880-411a-a217-e7d0206598d7			b4eb8841-196e-133a-e053-2a95a90a9400	2025-03-12	Warnings	Exact identifier spl set id: b4eb8841-196e-133a-e053-2a95a90a9400

Reported adverse events (FAERS/openFDA)#

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