Docusate Sodium Capsule, Liquid Filled
Product Images NDC 50268-268

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 50268-268). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avpak, 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

1 (Screen Shot 2017 05 17 At 11.10.07 Am)

1 (Screen Shot 2017 05 17 At 11.10.07 Am)
Drug Facts panel for Docusate Sodium 250 mg capsules, labeled as a stool softener. The active ingredient is docusate sodium 250 mg per softgel. Uses include relief of occasional constipation, prevention of dry hard stools, and generally producing a bowel movement within 12 to 72 hours. The label also includes packaging information, barcode, and AvPAK branding.*
FDA Label Image

2 (Screen Shot 2017 05 17 At 11.10.12 Am)

2 (Screen Shot 2017 05 17 At 11.10.12 Am)
Drug Facts panel for Docusate Sodium capsules providing warnings against use in certain conditions, instructions to consult a doctor before use or if specific symptoms occur, and directions for oral administration for adults and children 12 years and older, with a caution against use in children under 12 years unless directed by a doctor.*
FDA Label Image

3 (Screen Shot 2017 05 17 At 11.10.19 Am)

3 (Screen Shot 2017 05 17 At 11.10.19 Am)
Drug Facts panel for Docusate Sodium 250 mg capsules includes information on sodium content per softgel, storage instructions, an imprint code NV12 for identification, and a list of inactive ingredients. The label also provides a customer questions phone number and manufacturer details for AvKARE, Inc.*

* 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.