Stimulant Laxative Tablet, Delayed Release
Product Images NDC 69452-541

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Stimulant Laxative (NDC 69452-541). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bionpharma 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

Back (Back)

Drug Facts text panel providing usage directions, warnings, inactive ingredients, and contact information for a stimulant laxative bisacodyl 5 mg delayed-release oral tablet. It includes instructions on when to consult a doctor or pharmacist, usage directions by age, storage conditions, and a list of inactive ingredients.*

FDA Label Image

Front (Front)

Label for stimulant laxative bisacodyl delayed-release tablets USP 5 mg by BIONPHARMA INC. The label highlights 300 enteric-coated tablets with gentle, dependable constipation relief. Includes Drug Facts with active ingredient bisacodyl 5 mg per tablet, allergy alert for FD&C Yellow No. 5, and use for occasional constipation. The label also warns not to use if the printed safety seal is missing or torn.*

* 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.