Label: SENNA SYRUP- sennosides liquid
- NDC Code(s): 50268-731-11, 50268-731-24
- Packager: AVPAK
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 6, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- ASK DOCTOR
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
1 teaspoonful = 5 mL Directions: - Shake well before use
- Do not exceed recommended dose
Age Starting Dose Maximum Dosage Adults and children 12 years of age and over 2 to 3 teaspoonfuls (10 mL to 15 mL) once a day preferably at bedtime; increase as needed or as recommended by a doctor 3 teaspoonfuls (15 mL) in the morning and 3 teaspoonfuls (15 mL) at bedtime Children under 12 years of age Ask a doctor Ask a doctor - STORAGE AND HANDLING
- INACTIVE INGREDIENT
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
SENNA SYRUP
sennosides liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50268-731 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 METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PROPYLPARABEN (UNII: Z8IX2SC1OH) WATER (UNII: 059QF0KO0R) SUCRALOSE (UNII: 96K6UQ3ZD4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50268-731-24 24 in 1 BOX 05/03/2021 1 NDC:50268-731-11 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 M007 05/03/2021 Labeler - AVPAK (832926666)