Label: SENNA SYRUP- sennosides a and b syrup
- NDC Code(s): 66424-562-08
- Packager: SDA Laboratories, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 20, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient (in each 5 ml)
- Purpose
- Uses
-
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
• notice a sudden change in bowel movement that continues over a period of 2 weeks
Stop use and ask a doctor if
you have rectal bleeding or failure to have a bowel movement after use of laxative. These may indicate a serious condition
If pregnant or breast-feeding,ask a health professional before use
- KEEP OUT OF REACH OF CHILDREN
-
Directions
• shake well before use
• take preferably at bedtime or as directed by a doctorAge Starting Dose Maximum dosage adults and children
12 years and older
2-3 teaspoonfuls once a day 3 teaspoonfuls twice a day 6 years to under
12 years of age
1-1½ teaspoonfuls once a day 1½ teaspoonfuls twice
a day
2 to under 6 years
of age
1/2-3/4 teaspoon once a day 3/4 teaspoon twice a day under 2 years of age ask a doctor ask a doctor - Other information
- Inactive ingredient:
- QUESTIONS
- SPL UNCLASSIFIED SECTION
- Packaging
-
INGREDIENTS AND APPEARANCE
SENNA SYRUP
sennosides a and b syrupProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66424-562 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SENNOSIDES A AND B (UNII: 1B5FPI42EN) (SENNOSIDES A AND B - UNII:1B5FPI42EN) SENNOSIDES A AND B 8.8 mg in 5 mL Inactive Ingredients Ingredient Name Strength METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) SUCROSE (UNII: C151H8M554) WATER (UNII: 059QF0KO0R) Product Characteristics Color brown (dark brown) Score Shape Size Flavor CHOCOLATE Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66424-562-08 236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/01/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M007 01/01/2015 Labeler - SDA Laboratories, Inc. (948067889)
