Storage and handling
Other information Store at room temperature
STOPAIN COLD PAIN RELIEVING LIQUID SPRAY
- Manufacturer
- TROY MANUFACTURING, INC
- Effective date
- 2023-10-04
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:25:07
Label at a glance#
ProductSTOPAIN COLD PAIN RELIEVING
Active ingredientMENTHOL
Label structure14 sections
Contacts and useful links#
Websitewww.stopain.com
www.stopain.com
www.stopain.comWebsitewww.arthritis.org
www.arthritis.org
www.arthritis.orgLabel contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Drug Facts
Active Ingredient Purpose
Menthol 6.0% Topical Analgesic
Purpose
Topical Analgesic
INDICATIONS & USAGE SECTION
Uses: For the temporary relief of minor aches and pains of muscle and joints associated with - simple backache -arthritis - strains - bruises -sprains
WARNINGS SECTION
Warnings
For eternal use only. Avoid contact with eyes.
Flammable: Keep away from fire or flame
OTC - WHEN USING SECTION
When using this product
use only as directed
do not bandage tightly or use a heating pad
do not apply to wounds or damaged skin.
OTC - STOP USE SECTION
Stop use and ask a doctor if
condition worsens or 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.
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast feeding, aska health professional before use
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.
DOSAGE & ADMINISTRATION SECTION
Directions
Adults and children over 12 years: spray directly onto affected area without the need to rub, massage or bandage
repeat as necessary, but do not apply more than 4 times daily.
Children 12 years or younger: ask a doctor.
STORAGE AND HANDLING SECTION
Other information
Store at room temperature
INACTIVE INGREDIENT SECTION
Inactive Ingredients
Eucalyptus oil, isopropyl alcohol, peppermint oil, water
SPL UNCLASSIFIED SECTION
Manufactured for: Troy Healthcare, LLC 130 Lions Drive, Hazleton, PA 18202
800-201-PAIN (7246)
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
NOTHING LASTS LONGER
STOPAIN COLD
NO-DRIP, NO-STAIN
PAIN RELIEVING SPRAY
Immediate, Penetrating Pain Relief From
Arthritis
Muscle Aches
Back Pain
8fl oz (240 ml)
Your purchase benefits the Arthritis Foundation
Stopain. Exactly what it does. tm
Sprays at any Angle
Non Greasy
Light, pleasant scent
Easy to use
Works on contact
Pharmacist recommended
Our pharmacist recommended formulas:
Work on contact
Provide long-lasting pain relief
For more information, visit www.stopain.com today
made in USA
To report a serious adverse event, contact (800) 201 PAIN (7246)
Your purchase benefits the Arthritis Foundation
For every unit of Stopain(r) product sold, Troy Healthcare, LLC will donate a portion of the proceeds to the ARthrits Foundation with a minimum contribution of $25,000 to help people take control of arthritis. For information about arthritis, contact the Foundation at 800-283-7800 or www.arthritis.org.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| MENTHOL | ACTIVE INGREDIENT | L7T10EIP3A | 1 | |
| MENTHOL | ACTIVE MOIETY | L7T10EIP3A | 1 | |
| EUCALYPTUS OIL | INACTIVE INGREDIENT | 2R04ONI662 | 1 | |
| ISOPROPYL ALCOHOL | INACTIVE INGREDIENT | ND2M416302 | 1 | |
| PEPPERMINT OIL | INACTIVE INGREDIENT | AV092KU4JH | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Products#
Every source-derived product name is available through these pages.
- STOPAIN COLD PAIN RELIEVING
- MENTHOL
- EUCALYPTUS OIL
- ISOPROPYL ALCOHOL
- PEPPERMINT OIL
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 63936-8558 | 63936-8558-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| EUCALYPTUS OIL | 2R04ONI662 | IACT |
| ISOPROPYL ALCOHOL | ND2M416302 | IACT |
| PEPPERMINT OIL | AV092KU4JH | IACT |
| WATER | 059QF0KO0R | IACT |
| MENTHOL | L7T10EIP3A | ACTIB |
Source Document#
Inactive ingredient matches#
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| ISOPROPYL ALCOHOL | ISOPROPYL ALCOHOL | ND2M416302 | SPONGE / TOPICAL | 4 %w/w | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | CONCENTRATE / ORAL | 0.05 mg | ||
| ISOPROPYL ALCOHOL | ISOPROPYL ALCOHOL | ND2M416302 | SWAB / TOPICAL | 43.9 %w/w | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | SOLUTION / ORAL | 53 mg | ||
| ISOPROPYL ALCOHOL | ISOPROPYL ALCOHOL | ND2M416302 | LOTION, AUGMENTED / TOPICAL | 2070 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | FILM, SOLUBLE / BUCCAL | 3 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | POWDER, DENTIFRICE / DENTAL | NA | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | POWDER / SUBLINGUAL | 1 mg | ||
| ISOPROPYL ALCOHOL | ISOPROPYL ALCOHOL | ND2M416302 | TABLET, EXTENDED RELEASE / ORAL | NA | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | ELIXIR / ORAL | 0.04 mg/1ml | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | PASTE, DENTIFRICE / DENTAL | 49.3 %w/w | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | TABLET / SUBLINGUAL | 0.15 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | GUM, CHEWING / ORAL | 526 mg | ||
| ISOPROPYL ALCOHOL | ISOPROPYL ALCOHOL | ND2M416302 | OIL / AURICULAR (OTIC) | 6 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | SOLUTION / DENTAL | 0.04 %v/v | ||
| ISOPROPYL ALCOHOL | ISOPROPYL ALCOHOL | ND2M416302 | SOLUTION / TOPICAL | 40 %w/v | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | LOZENGE / ORAL | 12 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | CAPSULE / ORAL | 60 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | TABLET, ORALLY DISINTEGRATING / ORAL | 3 mg | ||
| ISOPROPYL ALCOHOL | ISOPROPYL ALCOHOL | ND2M416302 | OIL / TOPICAL | 72 mg | ||
| EUCALYPTUS OIL | EUCALYPTUS OIL | 2R04ONI662 | SYRUP / ORAL | NA | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | TABLET / ORAL | 28 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | SUSPENSION / ORAL | 100 mg/1ml | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | OINTMENT / TOPICAL | 0.2 %w/w | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | SHAMPOO / TOPICAL | 0.2 %w/w | ||
| ISOPROPYL ALCOHOL | ISOPROPYL ALCOHOL | ND2M416302 | GEL / TOPICAL | 75 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | SPRAY, METERED / SUBLINGUAL | 1 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | GUM, CHEWING / BUCCAL | 526 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | SYRUP / ORAL | 120 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | FILM / BUCCAL | 12 mg | ||
| ISOPROPYL ALCOHOL | ISOPROPYL ALCOHOL | ND2M416302 | GEL, METERED / TOPICAL | 525 mg |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 06ea3b0d-2e5d-d536-e063-6294a90a460c | d60d0d70-baf6-44b4-8a4e-2fa2716ca8c3 | 2023-10-04 | Warnings | 06ea3b0d-2e5d-d536-e063-6294a90a460c d60d0d70-baf6-44b4-8a4e-2fa2716ca8c3 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.