Active Ingredient (In Each Tablet)
Sennosides 8.6 mg
Senna Laxative Tablet
FDA Label NDC 72090-041
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Pioneer Life Sciences, Llc for the product Senna Laxative (NDC 72090-041). 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 active ingredient (in each tablet), purpose, uses:, warnings:, directions, other information, inactive ingredients, questions or comments?, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Laxative
Uses:
- relieves occasional constipation (irregularity).
- generally prodcues a bowel movement in 6-12 hours
Warnings:
Do not use
- Laxative products for longer than 1 week, unless directed by a doctor.
Directions
- Take preferably at bedtime or as directed by a doctor.
age | starting dosage | maximum dosage |
adults & children 12 years of age and over | 2 tablets once a day | 4 tablets twice a day |
children 6 to under 12 years | 1 tablet once a day | 2 tablets twice a day |
children 2 to under 6 years | 1 /2 tablet once a day | 1 tablet twice a day |
children under 2 years | ask a doctor | ask a doctor |
Other Information
- store at 20-25°C (68-77°F) excursions permitted between15°-30°C (59°-86°F)
- each tablet contains: Calcium 25 mg & sodium 3 mg
Inactive Ingredients
Lactose Monohydrate, Microcrysatlline Cellulose, Crosspovidone XL 10, PVP K30, Magnesium Stearate. Aqua Dry Clear contains: Polyvinyl alcohol, Polysorbate 80, Macrogol/PEG, Talc
Questions Or Comments?
Call + 1-732-994-2808 or email [email protected]
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