Erythromycin And Benzoyl Peroxide Gel
Product Images NDC 64980-328

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Erythromycin And Benzoyl Peroxide (NDC 64980-328). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rising Pharma Holdings, Inc., 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

233g Jar Carton

Packaging label for Erythromycin and Benzoyl Peroxide Topical Gel USP by Rising Pharma Holdings, Inc. The label indicates it is a prescription topical gel available in a 23.3 g jar. Strengths shown include 30 mg/g erythromycin and 50 mg/g benzoyl peroxide. The label contains usage instructions, storage conditions, and warnings for topical use only with Rx only designation.*

FDA Label Image

466 G Jar Carton

Packaging label for Erythromycin and Benzoyl Peroxide Topical Gel USP, labeled for topical use only and prescription use (Rx only). The label states the product is supplied in one 46.6g jar, with NDC 64980-328-02. The label includes manufacturer and distributor information for Lyne Laboratories, Inc. and Rising Pharmaceuticals, Inc., along with preparation, storage, and usage instructions.*

FDA Label Image

Label 2 (Benzoyl Peroxide Sf)

Chemical structure of benzoyl peroxide depicted as connected hexagonal and linear bonds showing the molecular arrangement of this active ingredient.*

FDA Label Image

Label (Erythromycin Sf)

Chemical structure diagram of erythromycin showing its molecular arrangement with multiple rings and functional groups, including methyl, hydroxyl, and ether groups, typical for this macrolide antibiotic.*

* 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.