SENNAZON- sennosides a and b syrup 
Bayshore Pharmaceuticals LLC [FL]

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.

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Sennazon Syrup

Drug Facts

Active Ingredient (in each teaspoonful)

Sennosides 8.8 mg

Purpose

Laxative

Uses

Warnings

Do not use

  • for longer than one week
  • when abdominal pain, nausea or vomiting are present

Ask a doctor before use if you have noticed a sudden change in bowel habits that lasts over two weeks

Ask a doctor or pharmacist before use if 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.

Stop use and ask a doctor if

  • you have rectal bleeding
  • you fail to have bowel movement after use of this product. These may indicate a serious condition.

If pregnant or breast-feeding ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

agestarting dosemaximum dosage
adults and children 12 years and older2 - 3 teaspoons once a day3 teaspoons twice a day
children 6 to under 12 years1 - 1 1/2 teaspoons once a day1 1/2 teaspoons twice a day
children 2 to under 6 years1/2 - 3/4 teaspoon once a day3/4 teaspoon twice a day
children under 2 yearsask a doctorask a doctor

Other information

Inactive ingredients

cocoa distillate flavor, natural chocolate flavor, methylparaben, propylene glycol, propylparaben, purified water, sucrose

Questions?

Call 1-855-bay-pharm 9 am - 5 pm EST Monday - Friday

Mfd. for: Bayshore Pharmaceuticals
Tampa, FL 33619

PRINCIPAL DISPLAY PANEL - 237 mL Bottle Label

NDC 76518-100-08

COMPARE TO ACTIVE
INGREDIENTS IN
SENOKOT®*

b
Protected

Sennazon
Syrup

Natural Vegetable LAXATIVE

Alcohol
Free

8 fl. oz. (237 mL)

PRINCIPAL DISPLAY PANEL - 237 mL Bottle Label
SENNAZON 
sennosides a and b syrup
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76518-100
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Sennosides A and B (UNII: 1B5FPI42EN) (Sennosides A and B - UNII:1B5FPI42EN) Sennosides A and B8.8 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
Methylparaben (UNII: A2I8C7HI9T)  
propylene glycol (UNII: 6DC9Q167V3)  
propylparaben (UNII: Z8IX2SC1OH)  
water (UNII: 059QF0KO0R)  
sucrose (UNII: C151H8M554)  
cocoa (UNII: D9108TZ9KG)  
Product Characteristics
ColorBROWNScore    
ShapeSize
FlavorCHOCOLATEImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76518-100-08237 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart33405/01/2012
Labeler - Bayshore Pharmaceuticals LLC [FL] (963298273)

Revised: 7/2013
Document Id: 28931b86-a3a1-42b5-a2df-45be00c37de3
Set id: 5d3106d5-ada2-4c98-8c99-f88df4849a56
Version: 2
Effective Time: 20130731
 
Bayshore Pharmaceuticals LLC [FL]