Erythromycin And Benzoyl Peroxide Kit
Product Images NDC 68682-900

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Erythromycin And Benzoyl Peroxide (NDC 68682-900). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Oceanside Pharmaceuticals, 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

Carton 23.3 G Gel.jpg

Packaging label for Erythromycin-Benzoyl Peroxide Topical Gel kit from Oceanside Pharmaceuticals. The label states that it is for topical use only and dispenses one 23.3 g jar. The label includes NDC 68682-900-23, directions for compounding the topical gel, storage conditions, warnings, and manufacturing information.*

FDA Label Image

Carton 46.6 G Gel.jpg

Packaging label for Erythromycin-Benzoyl Peroxide Topical Gel kit by Oceanside Pharmaceuticals. The label includes the product name, usage indication for topical use only, jar size of 46.6 g as dispensed, and instructions about reconstitution and storage. The label also contains barcode, NDC numbers, manufacturer details, and warnings for external use only and keeping out of reach of children.*

FDA Label Image

Label 0.8 G Erythromycin.jpg

Label for Erythromycin vial, part of the Erythromycin and Benzoyl Peroxide kit by Oceanside Pharmaceuticals. The label includes NDC 68682-924-08 and instructions for reconstituting erythromycin with 3 mL of 70% ethyl alcohol. It states storage instructions and warnings, with a net weight of 0.8 grams active erythromycin. Distributor information for Oceanside Pharmaceuticals in Bridgewater, NJ is also included.*

FDA Label Image

Label 1.6 G Erythromycin.jpg

Label for Erythromycin powder vial with NDC 68682-925-16, Rx only, distributed by Oceanside Pharmaceuticals. Instructions include adding 6 mL of 70% ethyl alcohol to dissolve erythromycin before combining with benzoyl peroxide topical gel. Net weight is 1.6 grams active erythromycin. Storage instructions specify refrigeration after reconstitution and a 3-month expiration date.*

FDA Label Image

Label 23.3 G Jar.jpg

Label for Erythromycin-Benzoyl Peroxide Topical Gel, a human prescription drug for topical use only. The label includes the NDC 68682-923-23 and indicates that the product contains one 23.3 g jar as dispensed. It details the active ingredients as erythromycin and benzoyl peroxide in a topical gel formulation, distributed by Oceanside Pharmaceuticals, a division of Bausch Health US, LLC, Bridgewater, NJ, and manufactured by Bausch Health Companies Inc. in Laval, Quebec, Canada. Additional usage and storage instructions are present.*

FDA Label Image

Label 46.6 G Jar.jpg

Label for Erythromycin-Benzoyl Peroxide Topical Gel, displaying the product name, dosage form as topical gel, and net quantity of one 46.6 g jar. The label indicates it is Rx only and for topical use only. It provides storage instructions and distributor information for Oceanside Pharmaceuticals and manufacturer details for Bausch Health Companies Inc.*

FDA Label Image

Chemical Structure (Erythromycin 02)

Chemical structure of Erythromycin and Benzoyl Peroxide, the active ingredients in the product. The image shows molecular diagrams representing the chemical composition of these compounds.*

FDA Label Image

Chemical Structure (Image 01)

Chemical structure diagram of the active ingredient for Erythromycin and Benzoyl Peroxide. The image shows molecular bonds and chemical groups characteristic of erythromycin, including multiple rings and functional groups.*

* 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.