Ddm Merthiolate
FDA Label NDC 53943-749

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Discount Drug Mart for the product Ddm Merthiolate (NDC 53943-749). 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 ddm merthiolate, active ingredient, purpose, indications, warnings, ask a doctor before use if you have, when using this product do not, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Ddm Merthiolate

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Indications

First aid antiseptic to help skin infection in minor: cuts, scrapes, burns, insect bites.

Warnings

For external use only.

Ask A Doctor Before Use If You Have

Deep or puncture wounds

Animal bites

Serious burns

When Using This Product Do Not

Get into the eyes

Apply over large areas of the body

Apply over raw surfaces or blistered areas

Use longer than one week unless directed by doctor.

Stop Use And Ask A Doctor If

Redness, swelling or pain persists or increases.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center immediately. Soap will deactivate the effects of this product.

Directions

  • Adults and children 2 years and older. Clean the affected area; apply a small amount on the area 1 to 3 times daily; may be covered with a sterile bandage. If bandaged, let dry first.
  • Children under 2 yrs. of age: Consult a doctor.

Inactive Ingredient

Acetone, FD&C Red No 4. Purified water.

* Please review the disclaimer below.