Otc - Active Ingredient
Active ingredients
Thuja Occidentalis 7C
Conzerol
FDA Label NDC 72383-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Discovery Pharma Sp Z O O for the product Conzerol (NDC 72383-000). 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, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, 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
Otc - Purpose
Purpose
MCV Relief
Otc - Keep Out Of Reach Of Children
Keep out of Reach of Children
Keep out of reach of children. If swallowed induce vomiting, get medical help or contact a Poison Control Center right away.
Indications & Usage
Molluscum Contagiosum lesion relief
Warnings
Warnings
- For externa use only
- Do not use on large areas of the body, wounds, punctured skin, in the eyes, animal bited or burns
- Stop use and ask doctor if rash or allergic reaction occurs/Condition worsens
- Keep out of reach of children. If swallowed induce vomiting, get medical help or contact a Poison Control Center right away
Dosage & Administration
Directions
- Clean infected skin area
- Apply small amount (equal to lesion size) on each lesion
- Gently run in circular motion leaving thin cream layer
- Repeat treatment 2 to 3 times daily
- Let dry for 3 minutes
Inactive Ingredient
Inactive Ingredients
Emulsifying Wax, Tea Tree Oil, Croton Lecleri, Clove Oil, Lemon Balm Oil
* Please review the disclaimer below.
