Clindamycin Phosphate Gel
Product Images NDC 72578-118

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 Clindamycin Phosphate (NDC 72578-118). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Viona Pharmaceuticals 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

Image (76fd5ef0 C06b 4f17 8607 89255693bffd 01)

Image (76fd5ef0 C06b 4f17 8607 89255693bffd 01)
Chemical structure diagram depicting the molecular composition of clindamycin phosphate, including atoms such as chlorine, methyl groups, hydroxyl groups, and phosphate moieties as part of the molecule's arrangement.*
FDA Label Image

Image 1 (76fd5ef0 C06b 4f17 8607 89255693bffd 02)

Image 1 (76fd5ef0 C06b 4f17 8607 89255693bffd 02)
Clindamycin Phosphate Gel, USP 1% topical gel in a 30 g package. Label shows usage instruction as 'For topical use only' and indicates Rx only. Manufactured by Zydus Lifesciences Ltd. and distributed by Viona Pharmaceuticals Inc. The label includes storage instructions, ingredients, and a barcode with NDC 72578-118-01.*
FDA Label Image

Image 2 (76fd5ef0 C06b 4f17 8607 89255693bffd 03)

Image 2 (76fd5ef0 C06b 4f17 8607 89255693bffd 03)
Packaging label for Clindamycin Phosphate Gel, USP 1%, a topical gel in a 30 g tube. The label includes dosage strength (1%), usage instructions (for topical use only), and manufacturer/distributor information: Zydus Lifesciences Ltd. and Viona Pharmaceuticals Inc. The label features storage instructions and a barcode, with the NDC code 72578-118-01 shown.*

* 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.