Stool Softener Docusate Sodium Capsule, Gelatin Coated
Product Images NDC 54257-902

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Stool Softener Docusate Sodium (NDC 54257-902). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Magno-humphries, 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.

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FDA Label Image

Label13 (Label13)

Label13 (Label13)
This is a drug information label for a laxative containing docusate sodium (100mg per softgel). It is indicated for relief of occasional constipation and typically produces bowel movement in 12-72 hours. The label contains important information about warnings, usage directions, and precautions. The user is advised not to use the laxative if presently taking mineral oil, unless directed to do so by a doctor. Users are also advised to see a doctor before use if they have stomach pain, nausea, vomiting, or sudden changes in bowel habits. The laxative should be taken as a single daily dose or in divided doses by adults and children over 12 years of age, while children aged between 2 to under 12 years of age are instructed to take one softgel every day. Children under two years should consult with a doctor before using the laxative. The inactive ingredients include FD&C red #40, FD&C yellow #6, gelatin, glycerin, polyethylene glycol, purified water, and sorbitol special. The product is distributed by Magno-Humphries Labs, Tigard, OR 97223. The statement "This product is not manufactured or distributed by the owner of the registered trademark ColaceĀ®" is also present.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.