Active Ingredient (Per 5 Ml)
Sennosides 8.8 mg
The following Structured Product Label (SPL) was submitted to the FDA by Kesin Pharma Corporation for the product Senna Syrup (NDC 81033-120). 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 (per 5 ml), purpose, uses, do not use, ask a doctor before use if you have, stop use and ask a doctor if, otc - keep out of reach of children, if pregnant or breast-feeding,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Sennosides 8.8 mg
Laxative
These could be a sign of a serious condition.
Keep out of reach of children.
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away.
| Age | Starting Dose | Maximun Dose |
| adults and children
12 years of age and over | 10 mL to 15 mL once a day
preferably at bedtime; increase as needed or as recommended by a doctor | 15 mL in the morning
and 15 mL at bedtime |
| children under 12 years of age | ask a doctor | ask a doctor |
NDC 81033-120-05: 5 mL unit dose cup
NDC 81033-120-50: Carton containing 50 (5 mL unit dose cups)
cherry flavor, citric acid, methylparaben, monoammonium glycyrrhizinate, potassium citrate, propylene glycol, propylparaben, purified water, sorbitol, sucralose
Call 1-833-537-4679
Packaged by:
Kesin Pharma
Oldsmar, FL 34677
Rev. 05/2025
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