MUSCLE RUB- menthol 2%, methyl salicylate 10% cream

Muscle Rub by

Drug Labeling and Warnings

Muscle Rub by is a Otc medication manufactured, distributed, or labeled by Derma Care Research Labs, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Menthol 2%, Methyl Salicylate 10%

PURPOSE

External Analgesic.

DOSAGE & ADMINISTRATION

For the temporary relief of itching associated with minor skin irritations and rashes due to eczema, insect bites, and poison oak.

WARNINGS

For external use only.

Do not use on wounds or damaged skin, or with a heating pad.

When using this product use only as directed, avoid contact with eyes or mucous membranes, do not bandage tightly.

Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days, if symptoms clear up and occur again within a few days, or if excessive skin irritation occurs.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

INDICATIONS & USAGE

Use only as directed, adults and children 12 years of age and older: apply to the affected area, not more than 3 to 4 times daily. Children . under 12 years of age: ask a doctor.

INACTIVE INGREDIENT

Aminomethyl Propanol, Carbomer, Cetyl Alcohol, Glycerin, Glyceryl Stearate, Isopropyl Palmitate, Potassium Cetyl Phosphate, Stearic Acid, Water.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MUSCLE RUB 
menthol 2%, methyl salicylate 10% cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72839-271
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	2 g  in 100 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	10 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETYL ALCOHOL (UNII: 936JST6JCN)
CHAMOMILE (UNII: FGL3685T2X)
DIMETHICONE 350 (UNII: 2Y53S6ATLU)
WATER (UNII: 059QF0KO0R)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
METHYL GLUCETH-20 (UNII: J3QD0LD11P)
GLYCERIN (UNII: PDC6A3C0OX)
PETROLATUM (UNII: 4T6H12BN9U)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
STEARETH-21 (UNII: 53J3F32P58)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72839-271-02	57 g in 1 TUBE; Type 0: Not a Combination Product	06/14/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	06/14/2019

Labeler - Derma Care Research Labs, LLC (116817470)