Promethegan Suppository
Product Images NDC 0713-0526

3 FDA label images from Cosette Pharmaceuticals, Inc. · 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 Promethegan (NDC 0713-0526). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cosette 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

12carton (12carton)

12carton (12carton)
The packaging label for PROMETHEGAN 12.5 mg suppositories features the brand name prominently with the active ingredient promethazine hydrochloride. It indicates the product is for rectal administration and contains 12 suppositories per package. The labeler is Cosette Pharmaceuticals, Inc., and storage instructions specify refrigeration between 2°-8°C. The package is white and dark green with black text, includes barcodes and Rx only designation.*
FDA Label Image

25carton (25carton)

25carton (25carton)
PROMETHEGAN 25 mg suppositories packaging label showing Promethazine HCl suppositories, USP for rectal administration. The label indicates a count of 12 suppositories per package, distributed by Cosette Pharmaceuticals, Inc., South Plainfield, NJ. The label includes dosage strength, route of administration, and storage instructions to refrigerate between 2°-8°C (36°-46°F). The packaging also states 'Rx Only' and has NDC code 0713-0526-12.*
FDA Label Image

Structural Formula (Structural Formula)

Structural Formula (Structural Formula)
Chemical structure of promethazine hydrochloride, showing the molecular arrangement with two aromatic rings, a sulfur atom, and a side chain containing an amine group.*

* 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.