Active Ingredient
Benzalkonium chloride 0.13%
Humco Merthiolate Liquid
FDA Label NDC 0395-8010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Humco Holding Group, Inc. for the product Humco Merthiolate (NDC 0395-8010). 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, ask a doctor before use if you have, when using this product, stop use and aska doctor if, keep out of reach of children, 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 skin infection in minor cuts, scrapes, burns and 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 eyes. If contact occurs, rinse eyes throughly with water. do not apply over large areas of the body. do not use over raw surfaces or blistered areas. do not use longer than 1 week unless directed by a doctor.
Stop Use And Aska Doctor If
condition persists or gets worse. symptoms 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 immediately.
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 it dry first. children under 2 years of age, do not use, consult a doctor.
Inactive Ingredients
Alcohol 10%, Acetone, FD&C Red No 4, purified water
Questions Or Comments?
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