Drug Facts: Active Ingredient
(in each suppository)
Bisacodyl 10 mg
The following Structured Product Label (SPL) was submitted to the FDA by Neilmed Pharmaceuticals Inc. for the product Bisacodyl Laxative (NDC 13709-328). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding drug facts: active ingredient, uses, warnings, do not use, ask a doctor before use, when using this product, stop use and ask a doctor if, if pregnant or breast-feeding,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
(in each suppository)
Bisacodyl 10 mg
if you have noticed a sudden change in bowel habits that lasts over a period of 2 weeks
it may cause abdominal discomfort, faintness, rectal bleeding and mild cramps
ask a health professional before use.
If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)
| Adults and children 12 and over | 1 suppository once daily |
| Children 6 to under 12 years | 1/2 suppository daily |
| Children under 6 years | Do not use |
hydrogenated vegetable oil
Adverse Drug Event Call: 1(877) 477-8633
Please do not discard this printed box and any enclosed printed material. The inside final product may not have all the details you require for the ongoing use of the product.
Purpose - Vasoconstrictor
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