Label: SENNA- sennosides liquid
- NDC Code(s): 60687-851-40, 60687-851-46, 60687-851-77
- Packager: American Health Packaging
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 25, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
-
Warnings
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 use
- Do not exceed recommended dose
Age
Starting Dose
Maximum dosage
Adults and children 12 years and older
2 to 3 unit dose cups once a day preferably at bedtime; increase as needed or as recommended by a doctor
3 unit dose cups in the morning and 3 unit dose cups at bedtime
Under 12 years of age
ask a doctor
ask a doctor
- Other Information
- Inactive Ingredients
- Questions or comments?
- Generic Section
- Principal Display Panel – Label – 8.8 mg/5 mL
- Principal Display Panel – Cup Lid – 8.8 mg/5 mL
-
INGREDIENTS AND APPEARANCE
SENNA
sennosides liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60687-851 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 ACETATE (UNII: DSO12WL7AU) 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:60687-851-77 4 in 1 CASE 11/17/2024 1 NDC:60687-851-46 10 in 1 TRAY 1 NDC:60687-851-40 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 NM900 11/17/2024 Labeler - American Health Packaging (929561009)