Obliterate
Product Images NDC 49520-101

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Obliterate (NDC 49520-101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mybody, 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

Obliterate_outer_box_drug Facts Panel (Obliterate Outer Box Drug Facts Panel)

Drug Facts panel for OBLITERATE containing active ingredient Benzoyl Peroxide 5% for acne treatment. Includes usage instructions, external use warnings, precautions such as avoiding eye contact and keeping out of reach of children, directions for application, storage information, inactive ingredients, and contact information for questions or comments. The labeler is mybody.*

FDA Label Image

Obliterate_outer_box_front (Obliterate Outer Box Front)

Packaging label for OBLITERATE Booster Pack: ACTIVE ACNE by mybody. The label indicates it is a step 2 mybooster product and includes a volume indication of 30 mL (2-1.0 fl oz US). The design is simple with the mybody logo in red and gray text on a white background with a red footer.*

FDA Label Image

Obliterate_inner Lbl (Obliterate Inner Lbl)

Label for OBLITERATE 2-in-1 Extreme Refining Solution containing 5% Benzoyl Peroxide by mybody. The 1 FL OZ (30 mL) product is indicated for acne treatment. The label includes usage instructions for morning and evening application, warnings for external use, and manufacturer contact details.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.