Docusate Sodium Liquid
Product Images NDC 0121-1870

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 0121-1870). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pai Holdings, Llc Dba Pai Pharma, 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

Principal Display Panel (5 mL Cup Tray Label)

Principal Display Panel (5 mL Cup Tray Label)
Label for Docusate Sodium Liquid 50 mg/5 mL, an oral stool softener laxative. The label indicates a 5 mL dosage delivery, alcohol-free and sugar-free formulation, packaged by Pharmaceutical Associates, Inc., Greenville, SC. The label includes an NDC number and a barcode, with a child-resistant packaging note.*
FDA Label Image

Principal Display Panel (10 mL Cup Tray Label)

Principal Display Panel (10 mL Cup Tray Label)
Docusate Sodium Liquid label showing 100 mg per 10 mL strength. The label indicates it is a stool softener laxative, alcohol free and sugar free, with a 10 mL delivery volume. Labeler is Pharmaceutical Associates, Inc., Greenville, SC. Barcode and NDC number 0121-1870-10 are visible.*
FDA Label Image

Principal Display Panel (16 fl oz (473 mL))

Principal Display Panel (16 fl oz (473 mL))
Label for Docusate Sodium Liquid 50 mg/5 mL oral solution by PAI Pharmaceutical Associates, Inc. The product is a stool softener laxative, alcohol and sugar free, in a 16 fl oz (473 mL) bottle. The label includes Drug Facts with active ingredient, uses, warnings, dosage directions by age group, and inactive ingredients.*

* 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.