Rugby ® Pain Relieving Cream Topical Analgesic

Manufacturer
Rugby Laboratories | Garcoa, Inc.
Effective date
2026-07-06
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-10-13 04:03:09

Label at a glance#

ProductRugby Pain Relieving Analgesic
Active ingredientMENTHOL, UNSPECIFIED FORM, Methyl Salicylate
Label structure10 sections

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.

Storage and handling

Store at room temperature.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active ingredients Purpose
Menthol 1.25%Topical Analgesic
Methyl Salicylate 15.0%Topical Analgesic

Use

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with

  • arthritis
  • simple backache
  • strains
  • sprains

Warnings

WARNINGS SECTION

For external use only

Allergy Alert

SPL UNCLASSIFIED SECTION

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

Do not use

OTC - DO NOT USE SECTION

  • immediately after shower or bath
  • with a heating pad
  • on wounds, damaged, broken or irritated skin

When using this product

OTC - WHEN USING SECTION

  • use only as directed
  • do not swallow
  • do not bandage tightly
  • avoid contact with eyes and mucous membranes

Stop and ask a doctor if

OTC - ASK DOCTOR SECTION

  • skin redness or irritation develops
  • condition worsens or pain lasts for more than 7 days

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast feeding, ask a 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 (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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.

Other information

STORAGE AND HANDLING SECTION

Store at room temperature.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Carbomer, Cetearyl Alcohol, Dimethicone, Glycerin, Methylparaben, Polysorbate 60, Propylparaben, Sodium Hydroxide, Sodium Lauryl Sulfate, Water

Questions or comments?

OTC - QUESTIONS SECTION

1-800-567-8600

SPL UNCLASSIFIED SECTION

Distributed by:
Rugby Laboratories
Indianapolis, IN 46268
(800) 616-2471

www.major-rugby.com

PRINCIPAL DISPLAY PANEL - 85 g Tube Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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)

Pain Cream
Pain Cream

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0536-14770536-1477-45

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22026-07-06daily-update2026-09-15 03:01:53
12026-07-06weekly-update2026-07-17 21:43:37

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
e40bb172-849c-4c65-bb89-de9f46d131f8be4ad54e-b647-489a-8057-6ab8a09d6b022026-07-06WarningsExact identifier
spl set id: be4ad54e-b647-489a-8057-6ab8a09d6b02

Reported adverse events (FAERS/openFDA)#

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