Mentholatum Ointment
FDA Label NDC 10742-0002

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by The Mentholatum Company for the product Mentholatum (NDC 10742-0002). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredients, purpose, uses, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Camphor 9%

Menthol 1.3%

Purpose

Camphor - Topical Analgesic

Menthol - Topical Analgesic

Uses

temporarily relieves minor aches and pains of muscles and joints

Warnings

For external use only

When Using This Product

  • do not get into eyes
  • do not apply to wounds or to damaged skin
  • do not bandage tightly
  • do not heat, microwave, or add to hot water as this may cause splattering and result in burns

Stop Use And Ask A Doctor If

  • condition worsens
  • symptoms persist for more than 7 days or clear up and occur again within a few days

Keep Out Of Reach Of Children.

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

Directions

  • adults and children 2 years and over: apply to affected area not more than 3 to 4 times daily
  • children under 2 years: ask a doctor

Inactive Ingredients

fragrance, petrolatum, titanium dioxide

Questions?

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