Eagle Brand Muscle Rub

Manufacturer
Borden Company (Private) Limited
Effective date
2026-04-27
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:55:03

Label at a glance#

ProductEagle Brand Muscle Rub
Active ingredientMENTHOL, METHYL SALICYLATE
Label structure9 sections

Indications and uses

For 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 12 years of age and older: apply to affected area not more than 3 to 4 times daily. ■ children under 12 years of age: do not use, consult a doctor.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

  • Menthol 14.5%
  • Methyl Salicylate 30%

Purpose

OTC - PURPOSE SECTION

External Analgesic

Uses

INDICATIONS & USAGE SECTION

For 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

When using this product

OTC - WHEN USING SECTION

  • Avoid getting into the eyes or mucous membranes.
  • Do not apply to wounds or damaged skin.
  • Do not bandage tightly.
  • Do not use otherwise than as directed.

Stop use and ask doctor if

OTC - WHEN USING SECTION

Condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor.

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 medical help or contact a Poison Control Centre right away.

Directions

DOSAGE & ADMINISTRATION SECTION

■ adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily.

■ children under 12 years of age: do not use, consult a doctor.

Other information

OTHER SAFETY INFORMATION

Store below 86 oF (30 oC).

Inactive ingredients

INACTIVE INGREDIENT SECTION

alcohol, camphor, fragrance, thymol

Questions?

OTC - QUESTIONS SECTION

If there are any questions or to report serious side effects, call 1-800-777-6717 or 1-800-645-0769.

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

85ml NDC: 43405-011-85

85ml Unit Box85ml Unit Box

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1654726menthol 14.5 % / methyl salicylate 30 % Topical SolutionPSN4
1654726menthol 145 MG/ML / methyl salicylate 300 MG/ML Topical SolutionSCD4
1654726menthol 14.5 % / methyl salicylate 30 % Topical SolutionSY4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43405-011-85Eagle BrandMuscle Rub1 in 1 BOXLIQUID14
43405-011-85Eagle BrandMuscle Rub85 mL in 1 BOTTLELIQUID854

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43405-01143405-011-85

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
Eagle Brand Muscle RubMENTHOL, METHYL SALICYLATEBorden Company (Private) Limited06cb845c-cc53-1f1d-e063-6394a90a8c012026-04-27WarningsExact identifier
ndc (package): 43405-011-85
ndc (product): 43405-011
ndc11 (package): 43405001185
spl id: 506bae39-6a3c-fd80-e063-6294a90ae2e7
spl set id: 06cb845c-cc53-1f1d-e063-6394a90a8c01

Reported adverse events (FAERS/openFDA)#

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