Package Label.Principal Display Panel
50 mL NDC: 77924-002-01
Benzoyl Peroxide
FDA Label NDC 77924-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Malezia Llc for the product Benzoyl Peroxide (NDC 77924-002). 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 package label.principal display panel, dosage & administration, warnings, inactive ingredient, otc - active ingredient, otc - purpose, indications & usage, otc - 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
Dosage & Administration
50 mL NDC: 77924-002-01
Warnings
50 mL NDC: 77924-002-01
Warning Section (Warnings)
Inactive Ingredient
50 mL NDC: 77924-002-01
Otc - Active Ingredient
50 mL NDC: 77924-002-01
Otc - Purpose
50 mL NDC: 77924-002-01
Purpose (Purpose)
Indications & Usage
50 mL NDC: 77924-002-01
Otc - Keep Out Of Reach Of Children
50 mL NDC: 77924-002-01
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