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Mentholatum Pain Relief Extra Strength

Dosage form: gel
Ingredients: MENTHOL 30mg in 1mL
Labeler: The Mentholatum Company
NDC Code: 10742-8134

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 ingredient

Menthol 3%


Topical analgesic


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

  • simple backache
  • arthritis
  • strains
  • sprains


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 to damaged or very sensitive skin
  • do not bandage tightly or cover with any type of wrap except clothing
  • do not bandage tightly

Stop use and ask a doctor if
  • condition worsens
  • excessive irritation, burning or discomfort 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 healthcare professional before use.

Keep Out of Reach of Children.

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

  • 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

Inactive ingredients

carbomer, iron oxides, isopropyl alcohol, methylparaben, mica, propylparaben, purified water, titanium dioxide, trolamine


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

Distributed by:

The Mentholatum Company

Orchard Park, NY 14127

Made in Canada

Package/Label Principal Display Panel

Mentholatum Pain Relief Extra Strength Gel

Package/Label Principal Display Panel

Distributed by:

The Mentholatum Company

Orchard Park, NY 14127

Made in Canada

menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10742-8134
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:10742-8134-1236 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34808/08/2011
Labeler - The Mentholatum Company (002105757)

Revised: 05/2011
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.