Clindamycin And Benzoyl Peroxide Gel
Product Images NDC 16714-984

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Clindamycin And Benzoyl Peroxide (NDC 16714-984). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rxllc, 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

25g-carton (25g Carton)

Clindamycin and Benzoyl Peroxide Gel 1%/5% topical gel packaging label. The label shows the product name and strength, instructions for reconstitution with clindamycin phosphate vial, and a 25 g jar size after reconstitution. It is labeled Rx only, manufactured for NorthStar Rx LLC, and includes storage instructions and pharmacist dispensing directions. Barcodes and manufacturing information are also visible.*

FDA Label Image

50g-carton (50g Carton)

Clindamycin and Benzoyl Peroxide Gel 1%/5% topical gel carton label. The label states it is for topical use only and must be reconstituted with clindamycin phosphate vial. The package contains one 50 g jar after reconstitution. It is manufactured for Northstar Rx LLC and made by Glenmark Pharmaceuticals Ltd. Dosage and storage instructions are included.*

FDA Label Image

Benzoyl-peroxide (Benzoyl Peroxide)

Chemical structure of clindamycin and benzoyl peroxide, showing the molecular arrangement with benzoyl peroxide clearly depicted as a key component of the compound.*

FDA Label Image

Clinidamycin-structure (Clinidamycin Structure)

Chemical structure diagram showing the molecular composition of an active ingredient in clindamycin and benzoyl peroxide gel, topical formulation by NorthStar RxLLC.*

* 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.