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Folrex Cream

Dosage form
CREAM
Labeler
Catalysis, SL
Label updated
2018-03-09
Retrieved
2026-09-07
Active ingredients
MENTHOL
View original label and images on DailyMed ↗
ACTIVE INGREDIENTS PURPOSE

Menthol 1.25%.................. External Analgesic

[Image in the official label — see DailyMed source]

Warnings
  • For external use only.
  • If conditions worsens, or if symptons persists for more than 7 days or clear up and recur within a few days, discontinue use of this product and consult a doctor.
  • Do not apply to wounds or damaged skins.
  • Do not bandaged tightly

WARNINGS

  • Avoid contact with eyes
  • Keep out of the reach of children. In case of overdose,get medical help or contact a Poison Control Medical Center inmediately

Warnings

Keep out of reach of children

Questions or comments?

+ 34 91 345 6902 M-F 9:00 am to 5:00 pm

Other Information

. keep the product in a cool and dry place

Directions
  • apply onto the affected area not more than 3 or 4 times daily
  • Children under 4 years old, consult with a Doctor.

복용법·사용법

  • apply onto the affected area not more than 3 or 4 times daily
  • Children under 4 years old, consult with a Doctor.
Uses
  • For the temporary relief of pains of minor aches and pain of muscles and joints associated with:
  • Simple backage, strains, bruises and sprains

Inactive Ingredients

Aqua, Caprylic/Capric Triglyceride, Cetyl Alcohol, Alcohol Denat, Glycerin, Cetearyl Alcohol, Dimethicone, Menthol, Ceteth-20, Phenoxyethanol., Steareth-20, Salicylic Acid , Sodium Metabisulfite, Diazolidinyl Urea, Folic Acid, Sodium Benzoate, Potassium Sorbate, Sodium Lauryl Sulfate, Sodium Cetearyl Sulfate, Ethylhexylglycerin., Citric Acid., Parfum. Coumarin, Hexyl Cinnamal, Linalool, Limonene, Geraniol, Hydroxycitronellal

Uses

For the temporary relief of pains of minor aches and pain of muscles and joints associated with:
Simple backage, strains, bruises and sprains

Package Label

[Image in the official label — see DailyMed source]

DailyMed Set ID: 6689c713-3731-0760-e053-2a91aa0aca30 · Version 2
NDC: 64539-014