Docusate Sodium Capsule, Liquid Filled
Product Images NDC 60687-129

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 Docusate Sodium (NDC 60687-129). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

0412901 0119 Docusate Sodium 100mg

0412901 0119 Docusate Sodium 100mg
Drug Facts panel for Docusate Sodium 100 mg softgels by American Health Packaging. Lists active ingredient, intended use as a stool softener laxative for occasional constipation, warnings, directions for dosing by age group, and storage instructions. Contains details on inactive ingredients and packaging information for 100 softgels (10 x 10).*
FDA Label Image

813de020 5779 3a2f E053 2a91aa0ae788

813de020 5779 3a2f E053 2a91aa0ae788
Docusate Sodium 100 mg liquid-filled capsules shown in red, oval shape. One capsule displays imprint "scu1" while the other shows a plain surface. This oral OTC drug is labeled by American Health Packaging.*
FDA Label Image

100 mg Docusate Sodium Softgel Blister (Card Print Docusate Sodium 100mg 10x10 712901)

100 mg Docusate Sodium Softgel Blister (Card Print Docusate Sodium 100mg 10x10 712901)
The image shows a sheet of multiple labels for Docusate Sodium 100 mg softgel capsules. Each label identifies the product as a stool softener laxative, includes the FDA NDC (60687-129-12), and displays American Health Packaging as the labeler based in Columbus, Ohio. The labels have space for expiry date and lot number.*

* 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.