Active Ingridients
Benzalkonium Chloride 0.13%
Mertodol Solution
FDA Label NDC 65055-201
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Laboratorios Jaloma, S.a. De C.v. for the product Mertodol Solution (NDC 65055-201). 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 ingridients, purpose, uses, warnings, keep out of the reach of children., directions., inactive ingredients, labels, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
First aid to help prevent infection in *minor cuts *scrapes *burns
Warnings
-For external use only
-Do not use in the eyes or apply over large areas of the body
Consult a doctor in case of
- deep or puncture wounds
-animal bites
-serious burns
-Stop use and consult a doctor if the condition persist or gets worse
-do not use longer than 1 week, unless directed by a doctor
Keep Out Of The Reach Of Children.
In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediatley.
Directions.
-Clean the affected area
-Apply a small amount of this product on the area 1 to 3 times daily
- May be covered with a sterile bandage
Inactive Ingredients
Acetone, Alcohol, d & c red No. 22, water.
* Please review the disclaimer below.
