Benzoyl Peroxide 10% Topical Wash Liquid
Product Images NDC 82461-313

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Benzoyl Peroxide 10% Topical Wash (NDC 82461-313). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medcore Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Label-1 (Benzoyl Peroxide 01)

Label-1 (Benzoyl Peroxide 01)
This is a medication label for a product containing 5% Benzoyl Peroxide, which is used for acne treatment. The instructions advise applying a thin layer to the affected area up to 3 to 4 times a day. It warns of possible skin irritation and dryness and provides guidance on how to manage these side effects. The label also includes information on storing the product and when to seek medical help.*
FDA Label Image

Label-1 (Benzoyl Peroxide 02)

Label-1 (Benzoyl Peroxide 02)
This text provides information about a skincare product containing 5% Benzoyl Peroxide for acne treatment. It includes details on how to use the product, warnings, directions, inactive ingredients, and contact details for the manufacturer. The product is recommended for external use only, and users are advised to avoid contact with eyes, lips, and mouth. It also includes instructions for use, storage information, and what to do in case of skin irritation or allergic reactions. The product is to be applied externally to the affected area up to 3-4 times a day for adults and children 2 years and older.*
FDA Label Image

Label-1 (Benzoyl Peroxide 03)

Label-1 (Benzoyl Peroxide 03)
This is a description of a skincare product labeled with the NDC number 82461-313-05. The product is a Benzoyl Peroxide 10% Acne Medication manufactured for Medcore LLC. It provides instructions for use, warnings, and directions for applying externally to the affected area up to 3 to 4 times a day for adults and children 2 years and older. The product also includes information on inactive ingredients, storage conditions, and contact details for inquiries. It is essential to keep the product out of reach of children and seek medical help if swallowed or in case of allergic reactions.*
FDA Label Image

Label-1 (Benzoyl Peroxide 04)

Label-1 (Benzoyl Peroxide 04)
This product is a Benzoyl Peroxide 10% acne medication manufactured by Medcore LLC. It is used for the treatment of acne. The drug facts included in the text provide information on the active ingredient, warnings, instructions for use, directions, other information, and inactive ingredients. It is recommended to clean the skin thoroughly before applying, to avoid excessive drying, and to gradually increase application if needed. The product should be stored at room temperature and protected from direct sunlight and excessive moisture. It is important to discontinue use if irritation occurs and seek medical advice. Additionally, it is essential to keep the product out of reach of children and seek medical help if swallowed.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.