Label: SENNA- sennosides a and b syrup
Contains inactivated NDC Code(s)
NDC Code(s): 17856-6289-5
- Packager: Atlantic Biologicals Corps
- This is a repackaged label.
- Source NDC Code(s): 0904-6289
- 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.
Updated May 4, 2016
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- Active Ingredient (in each teaspoonful)
Ask a doctor before use if you have
- stomach pain
- Noticed a sudden change in bowel movements that continues over a period of 2 weeks
you are taking any other drug. Take this product two or more hours before or after other drugs. Laxatives may affect how other drugs work. Ask a doctor or pharmacist before use if
you have rectal bleeding or fail to have bowel movement after use of laxative. These may indicate a serious condition. Stop use and ask a doctor if
Take preferably at bedtime or as directed by a doctor. Shake Well Before Using.
age starting dose maximum dosage adults and children 12 years and older 2 - 3 teaspoons once a day 3 teaspoons twice a day children 6 to under 12 years 1 - 1 1/2 teaspoons once a day 1 1/2 teaspoons twice a day children 2 to under 6 years 1/2 - 3/4 teaspoon once a day 3/4 teaspoon twice a day children under 2 years ask a doctor ask a doctor
- Other information
- Inactive ingredients
- SPL UNCLASSIFIED SECTION
- SENNA (SENNOSIDES A AND B) SYRUP
INGREDIENTS AND APPEARANCE
sennosides a and b syrup
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:17856-6289(NDC:0904-6289) 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) propylene glycol (UNII: 6DC9Q167V3) propylparaben (UNII: Z8IX2SC1OH) water (UNII: 059QF0KO0R) cocoa (UNII: D9108TZ9KG) sucrose (UNII: C151H8M554) Product Characteristics Color BROWN Score Shape Size Flavor CHOCOLATE Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:17856-6289-5 5 mL in 1 CUP; Type 0: Not a Combination Product 05/04/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part334 04/23/2012 Labeler - Atlantic Biologicals Corps (047437707) Registrant - Atlantic Biologicals Corps (047437707) Establishment Name Address ID/FEI Business Operations Atlantic Biologicals Corps 047437707 RELABEL(17856-6289) , REPACK(17856-6289)