FDA Label for Benzoyl Peroxide
View Indications, Usage & Precautions
Benzoyl Peroxide Product Label
The following document was submitted to the FDA by the labeler of this product Malezia Llc. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Package Label.Principal Display Panel
50 mL NDC: 77924-002-01
Dosage & Administration
50 mL NDC: 77924-002-01
Warnings
50 mL NDC: 77924-002-01
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
Indications & Usage
50 mL NDC: 77924-002-01
Otc - Keep Out Of Reach Of Children
50 mL NDC: 77924-002-01
* Please review the disclaimer below.