Nitroglycerin Ointment
Product Images NDC 52817-835

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nitroglycerin (NDC 52817-835). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Trupharma, Llc, 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 Description (Carton Nitroglycerin)

Image Description (Carton  Nitroglycerin)
Label for Nitroglycerin Ointment USP 0.4%, a rectal ointment containing 4 mg/g nitroglycerin. The product is distributed by TruPharma, LLC, and manufactured by Kavis Pharma LLC. The tube contains 30 grams of ointment. The label includes dosage instructions, storage conditions, and a dosage guide scale. The NDC is 52817-83530.*
FDA Label Image

Image-structure (Image Structure)

Image-structure (Image Structure)
Chemical structure of Nitroglycerin showing three carbon atoms each bonded to nitrate groups (ONO2). This depicts the molecular arrangement of the active ingredient Nitroglycerin found in the 4 mg/g ointment by Trupharma, LLC.*
FDA Label Image

Tube-1 (Tube 1)

Tube-1 (Tube 1)
Packaging carton for Nitroglycerin ointment 4 mg/g, rectal dosage form by Trupharma, LLC. The image shows a blank outline of the carton with dashed lines indicating dimensions and a dosage guide scale measured in inches for size reference.*
FDA Label Image

Tube-2 (Tube 2)

Tube-2 (Tube 2)
Packaging label for NITROGLYCERIN 4 mg/g ointment for rectal use, showing an outline of the carton with dosage guide markings. The label is associated with Trupharma, LLC and displays measuring guides indicating 1 inch increments on the carton.*

* 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.