Stopain Extra Strength Gel

Manufacturer
Troy Manufacturing, Inc.
Effective date
2025-07-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:08:20

Label at a glance#

ProductStopain Extra Strength Gel
Active ingredientMENTHOL
Label structure8 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints associated with: • simple backache • arthritis • strains • bruises • sprains

Dosage and administration

Adults and children 2 years of age and older:  • apply directly onto affected area, not more than 3 to 4 times daily • wash hands after use Children under 2 years of age: do not use, consult a doctor

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 8.0%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with: • simple backache • arthritis • strains • bruises • sprains

Warnings

WARNINGS SECTION

For external use only.Avoid contact with eyes.

Flammable: Keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

• use only as directed • do not bandage tightly or use a heating pad • do not apply to wounds or damaged skin

Stop use and ask a doctor if

OTC - STOP USE SECTION

• condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days • redness is present • excessive irritation of the skin develops

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

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

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 years of age and older: • apply directly onto affected area, not more than 3 to 4 times daily • wash hands after use

Children under 2 years of age:do not use, consult a doctor

Other Information

SPL UNCLASSIFIED SECTION

Store at room temperatur

Inactive Ingredients

INACTIVE INGREDIENT SECTION

acrylic acid/vinyl ester copolymer, dimethylsulfone (MSM), eucalyptus oil, glucosamine sulfate, hydroxypropylcellulose, PEG-8 dimethicone, pentylene glycol, peppermint oil, SD alcohol 39C, triethanolamine, water (USP) 

Questions or comments?

OTC - QUESTIONS SECTION

1-800-201-7246

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Inner PackageInner PackageLabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
283257menthol 8 % Topical GelPSN2
1541592Stopain COLD 8 % Topical GelPSN2
1541592menthol 0.08 MG/MG Topical Gel [Stopain]SBD2
283257menthol 0.08 MG/MG Topical GelSCD2
283257menthol 8 % Topical GelSY2
1541592Stopain 0.08 MG/MG Topical GelSY2
1541592Stopain 8 % Topical GelSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63936-8802-1Stopain Extra Strength Gel10 in 1 BOXGEL102
63936-8802-1Stopain Extra Strength Gel3 g in 1 PACKETGEL32

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63936-880263936-8802-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
Stopain Extra Strength GelMENTHOLTroy Manufacturing, Inc.8bb89002-d7a2-4bee-b5a5-1fd1949273ef2025-07-22WarningsExact identifier
ndc (package): 63936-8802-1
ndc (product): 63936-8802
ndc11 (package): 63936880201
spl id: 3a8599cf-1894-9687-e063-6294a90a4518
spl set id: 8bb89002-d7a2-4bee-b5a5-1fd1949273ef

Reported adverse events (FAERS/openFDA)#

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