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
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated March 15, 2021
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 (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 not final part334 01/01/2015 Labeler - SDA Laboratories, Inc. (948067889)
