Dosage and administration
adults and children 12 years and over: apply to affected area not more than 3 to 4 times daily children under 12 years: ask a doctor.
adults and children 12 years and over: apply to affected area not more than 3 to 4 times daily children under 12 years: ask a doctor.
Store at room temperature.
Drug Facts
| Active ingredients | Purpose |
|---|---|
| Menthol 1.25% | Topical Analgesic |
| Methyl Salicylate 15.0% | Topical Analgesic |
For the temporary relief of minor aches and pains of muscles and joints associated with
For external use only
Allergy Alert: If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.
If pregnant or breast feeding, ask a health professional before use
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Store at room temperature.
Carbomer, Cetearyl Alcohol, Dimethicone, Glycerin, Methylparaben, Polysorbate 60, Propylparaben, Sodium Hydroxide, Sodium Lauryl Sulfate, Water
1-800-567-8600
Distributed by:
Rugby Laboratories
Indianapolis, IN 46268
(800) 616-2471
NDC 0536-1477-45
Rugby®
MAXIMUM STRENGTH
PAIN RELIEVING CREAM
menthol 1.25%
topical analgesic
methyl salicylate 15%
topical analgesic
• helps provide relief from simple backache, arthritis, strains, bruises, and sprains
• powerful dual-action formula contains both menthol and methyl salicylate
Net Wt 3 oz (85 g)

Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 0536-1477 | 0536-1477-45 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MENTHOL, UNSPECIFIED FORM | L7T10EIP3A | ACTIB |
| Methyl Salicylate | LAV5U5022Y | ACTIB |
| CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED | K679OBS311 | IACT |
| Cetostearyl Alcohol | 2DMT128M1S | IACT |
| Dimethicone | 92RU3N3Y1O | IACT |
| Glycerin | PDC6A3C0OX | IACT |
| Methylparaben | A2I8C7HI9T | IACT |
| Polysorbate 60 | CAL22UVI4M | IACT |
| Propylparaben | Z8IX2SC1OH | IACT |
| Sodium Hydroxide | 55X04QC32I | IACT |
| Sodium Lauryl Sulfate | 368GB5141J | IACT |
| Water | 059QF0KO0R | IACT |
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 2 | 2026-07-06 | daily-update | 2026-09-15 03:01:53 |
| 1 | 2026-07-06 | weekly-update | 2026-07-17 21:43:37 |
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 |
|---|---|---|---|---|---|---|
| e40bb172-849c-4c65-bb89-de9f46d131f8 | be4ad54e-b647-489a-8057-6ab8a09d6b02 | 2026-07-06 | Warnings | be4ad54e-b647-489a-8057-6ab8a09d6b02 |
Adverse event summaries are temporarily unavailable. Other product information remains available.