Acne Wipeout All Day Breakout Control
Product Images NDC 50544-152

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Acne Wipeout All Day Breakout Control (NDC 50544-152). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by University Medical Pharmaceuticals Corp., 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

Hydrate1 (50544152 1)

Packaging label for ACNE WIPEOUT ALL DAY BREAKOUT CONTROL Hydrating Cream by University Medical Pharmaceuticals Corp. The product features 5% benzoyl peroxide acne treatment in a 2 FL OZ (60 mL) tube. The label describes it as time-released, non-comedogenic, fragrance-free, and paraben-free. The packaging includes the product name, usage indication as a hydrating cream for acne care, and manufacturer information. Additional text details warnings, directions, and inactive ingredients.*

* 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.