EAGLE BRAND MUSCLE RUB- menthol, methyl salicylate liquid

Drug Labeling and Warnings

Drug Details [pdf]

Active ingredients

• Menthol 14.5%
• Methyl Salicylate 30%

Purpose

External Analgesic

Uses

For the temporary relief of minor aches and pains of muscles and joints associated with ■ simple backache ■ arthritis ■ strains ■ bruises ■ sprains.

Warnings

For external use only

When using this product

• Avoid getting into the eyes or on mucous membranes.
• Do not apply to wounds or damage skin.
• Do not bandage tightly.
• Do not use if excessive irritation of the skin develops.
• Do not use otherwise than as directed.

Stop use and ask doctor if

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 beast-feeding

Ask a health professional before use.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• 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

Store below 86 oF (30 oC).

Inactive ingredients

alcohol, camphor, fragrance, thymol

Questions?

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

Package Label

85ml NDC: 60954-019-85

INGREDIENTS AND APPEARANCE

EAGLE BRAND  MUSCLE RUB
menthol, methyl salicylate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60954-019
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	30 g  in 100 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	14.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
THYMOL (UNII: 3J50XA376E)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60954-019-85	1 in 1 BOX	04/01/2026
1		85 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	04/01/2026

Labeler - PT. EAGLE INDO PHARMA (728682519)

Establishment
Name	Address	ID/FEI	Business Operations
PT. EAGLE INDO PHARMA		728682519	manufacture(60954-019)