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Mentholatum Pain Relief Muscle Rub

Dosage form: cream
Ingredients: MENTHOL 59.1mg in 1g, METHYL SALICYLATE 128mg in 1g
Labeler: The Mentholatum Company
NDC Code: 10742-8120

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts

Active ingredients

Menthol 5.91%

Methyl salicylate 12.8%

Purpose

Menthol - Topical analgesic

Methyl salicylate - Topical analgesic

Uses

temporarily relieves minor aches and pains of muscles and joints due to

  • arthritis
  • strains
  • simple backache
  • sprains
  • bruises

Warnings

For external use only

When using this product
  • use only as directed
  • do not get into eyes or on mucous membranes
  • do not apply to wounds or damaged skin
  • do not bandage tightly
  • do not use with a heating pad, other heat sources, or right after a shower / bath
  • do not use in combination with other external analgesic products

Stop use and ask a doctor if
  • condition worsens
  • excessive irritation of the skin develops
  • symptoms persist for more than 7 days or clear up and occur again within a few days

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 right away.

Directions
  • adults and children 12 years and over: apply a thin layer to affected area not more than 3 to 4 times daily
  • avoid overuse on large areas of the skin
  • children under 12 years: ask a doctor

Inactive ingredients

cetostearyl alcohol, eucalyptus globulus leaf oil, lanolin, light mineral oil, propylene glycol, purified water, quaternium-15, sodium cetearyl sulfate

Questions?

Toll free 1-877-636-2677 MON - FRI 9 AM to 5 PM (EST) www.mentholatum.com

Package/Label Principal Display Panel

The Mentholatum Company

Orchard Park, NY 14127

MENTHOLATUM PAIN RELIEF MUSCLE RUB 
menthol, methyl salicylate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10742-8120
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (MENTHOL) MENTHOL59.1 mg  in 1 g
METHYL SALICYLATE (METHYL SALICYLATE) METHYL SALICYLATE128 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CETOSTEARYL ALCOHOL 
EUCALYPTUS OIL 
LANOLIN 
LIGHT MINERAL OIL 
PROPYLENE GLYCOL 
WATER 
QUATERNIUM-15 
SODIUM CETOSTEARYL SULFATE 
Packaging
#Item CodePackage Description
1NDC:10742-8120-11 TUBE (TUBE) in 1 CARTON
135 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34810/03/2011
Labeler - The Mentholatum Company (002105757)

Revised: 10/2011
 
The Mentholatum Company

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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