Label: SENNA- sennosides liquid
- NDC Code(s): 0904-7528-41, 0904-7528-94
- Packager: Major Pharmaceuticals
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 18, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient (per teaspoonful - 5 mL) Purpose
- Uses
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Warnings
Do not use
• laxative products for longer than 1 week unless directed by a doctor.
Ask a doctor or pharmacist before use if you have
• stomach pain • nausea • vomiting
• noticed a change in bowel movement that continues over a period of 2 weeks -
Directions
• shake well before using • Do not exceed recommended dose
Age Starting Dose Maximum Dose adults and children 12 years
and older2 to 3 teaspoonfuls once a day preferably at bedtime; increase as needed or as recommended by a doctor 3 teaspoons in the morning and 3 teaspoons at bedtime Under 12 years of age ask a doctor ask a doctor
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Other Information
- store at room temperature 20° to 25°C (68° to 77°F).
- a brown, natural flavored syrup supplied in the following oral dosage form:
NDC 0904-7528-41: 5 mL unit dose cup, in a tray of ten cups.
NDC 0904-7528-94: Case contains 40 unit dose cups of 5 mL (0904-7528-41) packaged in 4 trays of 10 unit dose cups each. - Inactive ingredients:
- Questions or comments?
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- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
SENNA
sennosides liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0904-7528 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES 8.8 mg in 5 mL Inactive Ingredients Ingredient Name Strength CITRIC ACID (UNII: 2968PHW8QP) GLYCERIN (UNII: PDC6A3C0OX) METHYLPARABEN (UNII: A2I8C7HI9T) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) PROPYLPARABEN (UNII: Z8IX2SC1OH) WATER (UNII: 059QF0KO0R) SUCROSE (UNII: C151H8M554) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0904-7528-94 4 in 1 CASE 03/06/2025 1 10 in 1 TRAY 1 NDC:0904-7528-41 5 mL in 1 CUP, UNIT-DOSE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M008 03/06/2025 Labeler - Major Pharmaceuticals (191427277)

