Broda Acne Gel
Product Images NDC 54111-112

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Broda Acne (NDC 54111-112). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bentley Laboratories, 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

Broda Acne Spot1 (Broda Acne Spot1)

Broda Acne Spot1 (Broda Acne Spot1)
BRODA Acne Treatment Pen, Anti-acne IntelliGel topical gel packaging label. Highlights IntelliGel Technology with 2% beta hydroxy acid. The label states it forms an invisible TrueSkin patch, is alcohol-free hydrogel, and does not cause peeling or flaking. Net weight is 0.071 oz (2 g), with branding prominently showing BRODA Anti-Acne IntelliGel.*
FDA Label Image

Broda Acnespot2 (Broda Acne Spot2)

Broda Acnespot2 (Broda Acne Spot2)
BRODA Acne Spot Treatment Gel, alcohol-free hydrogel, in a 20 g (0.71 oz) package. The label highlights anti-acne IntelliGel technology with maximum strength 2% beta hydroxy acid, claims of no peeling or flaking, and forms a TrueSkin invisible patch. Distributed by Broda International, LLC.*
FDA Label Image

Broda Acnespot3 (Broda Acne Spot3)

Broda Acnespot3 (Broda Acne Spot3)
Drug Facts panel for BRODA Anti-acne IntelliGel topical gel with 2% salicylic acid acne treatment. The label provides active ingredient, uses for acne treatment, warnings for external use, directions for application, and inactive ingredients including water, poloxamer 407, propylene glycol, PEG-400, laureth-4, menthol, and bisabolol. It also mentions IntelliGel technology and suitability for sensitive skin with alcohol-free hydrogel.*

* 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.