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Pasmol Pain Relieving

Dosage form: cream
Ingredients: MENTHOL 5g in 100g, METHYL SALICYLATE 14g in 100g
Labeler: Grafor, Inc.
NDC Code: 61361-820

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.

Pasmol Pain Relieving Ointment

Active ingredients

Menthol 5%

Methyl Salicylate 14%

Purpose

Pain Relieving

Uses

For the temporary relief of minor aches and pains of the muscles and joints associated with:

  • Arthritis
  • simple backache
  • bruises
  • sprains

Warnings

For external use only.

Do not use
  • in the eyes
  • on mucous membranes
  • on wounds or damaged skin

When using this product
  • do not bandage tightly

Stop use and ask a doctor if
  • condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few day
  • redness is present

  • excessive irritation of the skin develops

Keep out of reach of children

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

Directions
  • Adults and children three years of age and older: apply to affected area not more than 3-4 times daily.
  • Children under 3 years of age: consult a doctor

Inactive ingredients

PETROLATUM

MANUFACTURED BY GRAFOR INC. 1360 CASTELLANAS ST LA RAMBLA PONCE, PR 00730 UNITED STATES (787) 842-1423 WWW.PASMOL.COM REPORT ADVERSE EVENTS TO GRAFOR INC.

Pasmol Pain Relieving Ointment, 85g (61361-820-03)

PASMOL

“Arthritis Formula”

“Formula Artritis”

Pain Relieving Ointment

Net Wt./ Peso Neto 3 oz (85 g)

PASMOL PAIN RELIEVING 
menthol and methyl salicylate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61361-820
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (MENTHOL) MENTHOL5 g  in 100 g
METHYL SALICYLATE (SALICYLIC ACID) METHYL SALICYLATE14 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
PETROLATUM 
Packaging
#Item CodePackage Description
1NDC:61361-820-0385 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34804/08/2015
Labeler - Grafor, Inc. (135138811)
Establishment
NameAddressID/FEIOperations
Grafor, Inc.135138811manufacture(61361-820)

Revised: 04/2015
 
Grafor, Inc.

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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