Otc - Active Ingredient
Eugenia caryophylata 60% w/w
Santalum Spicatum 0.2% w/w
Mollenol
FDA Label NDC 72269-019
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jeva Laboratories for the product Mollenol (NDC 72269-019). 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 otc - active ingredient, inactive ingredient, indications & usage, otc - purpose, dosage & administration, warnings, otc - keep out of reach of children, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Coconut Oil
Indications & Usage
MCV relief
Molluscum contagiosum lesion relief.
Otc - Purpose
MCV Relief
Dosage & Administration
Apply 2 times daily directly to each molluscum
Do not rub in.
Cover with bandage if possible.
Warnings
For external use only.
Keep out of reach of children.
Do not use on wounds, punctured skin or near or in eyes.
Stop use and ask doctor if rash or allergic reaction occurs or condition worsens.
If swallowed induce vomit, seek medical help, or contact a Poison Control Center right away.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Package Label.Principal Display Panel
Mollenol (Mollenol)
* Please review the disclaimer below.
