Dosage and administration
Clean and dry affected area remove patch from film apply to affected area not more than 3 to 4 times daily remove patch from the skin afer a maximum of 8 hours application
Clean and dry affected area remove patch from film apply to affected area not more than 3 to 4 times daily remove patch from the skin afer a maximum of 8 hours application
Camphor 3.1%
Menthol 6.0%
Methyl Salicylate 10.0%
Topical Analgesic
For the temporary relief of minor aches and pains of muscles & joints associated with:
For external use only.
Allergy alert: If prone to allergic reaction from asirin or salicylates, consult a doctor before use
Do not use
ask a health professional before use.
If swallowed,get medical help or contact a Poison Control Center right away. Store new and dispose of used product out of reach of children.
Polyethylene, Acrylic adhesive
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71662-003-60 | Re-Lieved 3 in 1 Patch | 19 mg in 1 POUCH | PATCH | 19 | 2 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 71662-003 | 71662-003-60 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) | 1PEZ3NLY6I | IACT |
| SILICON DIOXIDE | ETJ7Z6XBU4 | IACT |
| MENTHOL, (+)- | C6B1OE8P3W | ACTIB |
| CAMPHOR (SYNTHETIC) | 5TJD82A1ET | ACTIB |
| METHYL SALICYLATE | LAV5U5022Y | ACTIB |
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 |
|---|---|---|---|---|---|---|
| Re-Lieved 3 in 1 Patch | MENTHOL, CAMPHOR, METHYL SALICYLATE PATCH | Transfer Technology | e9ab9a03-b9e3-7317-e053-2995a90a9950 | 2025-01-11 | Warnings | 71662-003-60 71662-003 71662000360 2b743728-1f2c-4ba8-e063-6294a90a74a2 e9ab9a03-b9e3-7317-e053-2995a90a9950 |
Adverse event summaries are temporarily unavailable. Other product information remains available.