Senna Tablet
Product Images NDC 71399-1017

View Photos of 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 Senna (NDC 71399-1017). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Akron Pharma 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

100ud (86 100 Ud)

100ud (86 100 Ud)
Senna Tablets, 8.6 mg Sennosides, natural vegetable laxative oral tablets in a 100-count package by Akron Pharma Inc. The yellow-green carton prominently displays the product name, active ingredient strength, and unit dose form. The label states 'Compare to the active ingredient in Senokot Tablets' and highlights gentle relief of constipation. Additional labeling includes Drug Facts and manufacturer information.*
FDA Label Image

100 (86 100)

100 (86 100)
Senna Tablets 8.6 mg, oral natural vegetable laxative containing sennosides, packaging shows 100 tablets. Label displays active ingredient, usage, warnings, dosing directions, inactive ingredients, and storage instructions. Manufactured by Akron Pharma Inc. with NDC 71399-1017-1.*
FDA Label Image

1000 (86 1000)

1000 (86 1000)
Drug Facts panel for Senna Tablets containing 8.6 mg of Sennosides per tablet, labeled as a natural vegetable laxative. The panel details active ingredient, uses, warnings, directions for different age groups, other product information including calcium content, storage instructions, and a list of inactive ingredients. Manufacturer and distributor information, barcode, and tamper-evident warnings are also present.*

* 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.