Tincture Merthiolate Tincture
FDA Label NDC 24286-1532

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Dlc Laboratories, Inc for the product Tincture Merthiolate (NDC 24286-1532). 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 ingredient, purpose, uses, warnings, when using this product, stop use and consult 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.

Active Ingredient

Benzalkonium chloride 0.13%

Uses

first aid to help prevent infection in minor:
cuts - scrapes - burns - insect bites

Warnings

For external use only.
Consult a doctor before use if you have - deep or puncture wounds - animal bites - serious burns

Directions

  • adults and children 2 years of age and older: clean the affected area
  • apply a small amount of this product to the area using the enclosed applicator or a cotton-tipped applicator 1 to 3 times daily _ may be covered with a sterile bandage (let dry first)
  • children under 2 years, ask a doctor

Other Information

  • medication will stain skin and clothing

Inactive Ingredients

acetone, alcohol, DandC red no. 22, purified water

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