Iodine
Product Images NDC 16638-166

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Iodine (NDC 16638-166). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Borisovskiy Zavod Medicinskikh Preparatov Jsc, 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 Of Group Label 1 (Group Label 1)

This is a description of a pharmaceutical product consisting of 165 vials of iodine in alcoholic solution for external applications. The vials have a group label dimension of 60 x 90 mm and the product is manufactured by JSC "Borisovskiy Zavod Medicinskikh Preparatov" located at Chapaeva str. 64, Borisov, 222518, Republic of Belarus. The product has a batch number and shelf life information. Additionally, there is a graphic design version number indicating the use of Pantone Black C and Pantone 1505 C.*

FDA Label Image

Image Of Group Label 2 (Group Label 2)

This is a description of a group label (60 x 90 mm) for 55 vials (10 ml each) of Iodine 10 ml - alcoholic solution for external applications. The label includes the manufacturer's details (NDC 16638-166-38 1SC "BORISOVSKIY ZAVOD MEDICINSKIKH PREPARATOV" & Chapaeva str. 64, Borisov, 222518, Republic of Belarus), batch number, shelf life, and graphic design version number. The label also mentions the use of Pantone Black C and Pantone 1505 C as colors.*

FDA Label Image

Image Of Vial Label (Vial Label)

This is a label, with a size of 22 x 60 mm, which includes information about two Pantone colors: Black C and 1505 C. Additionally, it mentions a "Graphic design version number."*

* 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.