Anti-diarrheal Tablet
Product Images NDC 37835-131

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Anti-diarrheal (NDC 37835-131). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bi-mart, 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

100 (Loperamide 100)

The packaging label for BI-MART Anti-diarrheal tablets contains Loperamide Hydrochloride 2 mg, noted as original prescription strength. It highlights control of diarrhea symptoms and traveler’s diarrhea. The label includes dosage form as caplets, 100 count, and the NDC 37835-131-01. Warnings and use instructions are partially visible on the right side.*

FDA Label Image

12 (Loperamide 12)

Box label for BI-MART Anti-Diarrheal Caplets containing Loperamide Hydrochloride Tablets, 2 mg. The label states it controls symptoms of diarrhea, original prescription strength, with a package size of 12 caplets. The label also includes Drug Facts, Directions, and active ingredient information. BI-MART is the labeler.*

FDA Label Image

24 (Loperamide 24)

The carton label for BI-MART Anti-Diarrheal Caplets contains Loperamide Hydrochloride Tablets, 2 mg, with 24 caplets per package. The front features the BI-MART brand name prominently in red, the product name in black and blue text, and a depiction of one greenish caplet. The label includes drug facts, directions, and warnings on the side panels. The labeler is BI-MART, and the package includes standard over-the-counter drug information and barcodes.*

* 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.