Oraltag
Product Images NDC 54702-501

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Oraltag (NDC 54702-501). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Interpharma Praha, A.s., 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

Principal Display Panel (Pouch Label Back)

Instructions for use of ORALTAG (iohexol) oral solution, showing a four-step illustrated guide: adding water or beverage to the fill line on the bottle, replacing the cap and shaking to dissolve the powder, the dose ready for patient consumption, and discarding any unused portion.*

FDA Label Image

Principal Display Panel (Pouch Label Front)

ORALTAG (iohexol) for oral solution label shows it contains a single-use bottle with 9.7 g of iohexol powder, equivalent to 4.5 g of carbon bound iodine. The label indicates nonsterile formulation, for oral use only, manufactured for Interpharma Praha, a.s., Prague, Czech Republic by Ultra Seal Corporation, New Paltz, New York. Storage conditions and barcode are present.*

FDA Label Image

Chemical Structure (Iohexol Structure)

Chemical structure of the active ingredient in the ORALTAG product by Interpharma Praha, a.s., showing its molecular composition and connectivity including iodine, oxygen, nitrogen, and hydroxyl groups.*

FDA Label Image

Principal Display Panel (Bottle Label)

ORALTAG (iohexol) oral solution label showing concentrations from 9 mg/mL to 21 mg/mL and volume measurements from 214 mL to 500 mL. The label states 9.7 g of iohexol per bottle with equivalent 4.5 g carbon bound iodine, single use bottle with discard unused portion, and concentration range of prepared solution 9-21 mg/mL. Label indicates for oral use only, nonsterile, manufactured by Interpharma Praha, a.s., and includes handling and storage instructions along with the Rx only designation.*

* 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.