Senna-s Tablet, Film Coated
Product Images NDC 81005-102

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Senna-s (NDC 81005-102). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aarkish Pharmaceuticals Nj 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.

Product Images & Figures Index

FDA Label Image

Sennosides And Docusate Sodium Tablets 300 Counts (Senna Plus Cont Label 1)

Sennosides And Docusate Sodium Tablets 300 Counts (Senna Plus Cont Label 1)
Senna-S film-coated tablet label showing the product contains Sennosides 8.6 mg and Docusate Sodium 50 mg as active ingredients. It is a natural vegetable laxative ingredient plus stool softener. The label indicates a package size of 300 tablets, manufactured by Aarkish Pharmaceuticals NJ Inc. The label includes dosage instructions, warnings, and inactive ingredients list. It also displays Eagle Health Pharma branding and a barcode.*
FDA Label Image

Sennosides And Docusate Sodium Tablets 1000 Counts (Senna Plus Cont Label 2)

Sennosides And Docusate Sodium Tablets 1000 Counts (Senna Plus Cont Label 2)
The image shows the front and side label of Senna-S tablets, a film-coated oral tablet containing Docusate Sodium 50 mg and Sennosides 8.6 mg. The product is a natural vegetable laxative and stool softener for overnight constipation relief. The package contains 1000 tablets and is labeled by Eagle Health Pharma, manufactured by Aarkish Pharmaceuticals NJ Inc. It includes warnings, directions, and inactive ingredients information.*

* 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.