Active Ingredient
Miconazole nitrate 2%
The following Structured Product Label (SPL) was submitted to the FDA by Laboratorios Liomont, S.a. De C.v. for the product Conazol (NDC 59208-001). 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, do not use, when using this product, stop use and ask a doctor if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Miconazole nitrate 2%
Antifungal
For external use only
on children less than 2 years of age unless directed by a doctor
• avoid contact with the eyes
If swallowed, get medical help or contact a Poison Control Center right away.
and socks at least once daily
butylated hydroxyanisole, caprylic/capic triglyceride,carbomer 980, emulsifying wax, glycerin, methylparaben, propylene glycol, propylparaben, purified water, triethanolamine
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