SENNA PLUS- standardized senna concentrate and docusate sodium tablet, film coated 
Cardinal Health

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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SENNA PLUS Tablets 8.6/50 mg

Active ingredient

Drug Facts

Active Ingredients (in each tablet)

Docusate sodium 50 mg

Sennosides 8.6 mg

Generic Section

Standardized Senna Concentrate & Docusate Sodium

Purpose

Stool Softener

Stimulant Laxative

Uses

relieves occasional constipation
generally produces bowel movement in 6-12 hours

Warnings

Do not use

if you are taking mineral oil
for longer than one week
when abdominal pain, nausea or vomiting are present

Ask a doctor before use if you have 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 a bowel movement after use of this product.

These may indicate a serious condition.

This Unit Dose package is not child resistant and is intended for institutional use only.

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

Keep out of the reach of children.

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

Directions

 Take preferably at bedtime or as directed by a doctor
if you do not have a comfortable bowel movement by the second day, increase dose by one tablet (do not exceed maximum dosage)

 age

 starting dosage

 maximum dosage

 adults and children 12 years & over

 2 tablets once daily

 4 tablets twice daily

 children 6 to under 12 years

 1 tablet once daily

 2 tablets twice daily

 children 2 to under 6 years

 1/2 tablet once daily

 1 tablet twice daily

 children under 2 years

 ask a doctor

 ask a doctor

Other Information

each tablet contains:  calcium 20 mg, sodium 6 mg (LOW SODIUM)
store at 20º - 25ºC (68º - 77ºF) 

Inactive ingredients

carnauba wax, colloidal silicon dioxide, croscarmellose sodium, D&C yellow #10 aluminum lake, dibasic calcium phosphate dihydrate, FD&C yellow #6 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, sodium benzoate, stearic acid, titanium dioxide

Questions or comments?

(800) 616-2471 

Distributed by

Distributed by

MAJOR® PHARMACEUTICALS

17177 N Laurel Park Dr., Suite 233

Livonia, MI  48152 USA

Distributed by

Cardinal Health

Dublin, OH 43017

L4928487-10318

L4928487-20318

Principal Display Panel

Senna Plus Tablets 8.6/50 mg

Standardized Senna Concentrate

& Docusate Sodium

10 Tablets

bag label
SENNA PLUS 
standardized senna concentrate and docusate sodium tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55154-5889(NDC:0904-6339)
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 B8.6 mg
DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM50 mg
Inactive Ingredients
Ingredient NameStrength
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
MINERAL OIL (UNII: T5L8T28FGP)  
AMMONIUM LAURETH-5 SULFATE (UNII: 43ZIH89I48)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
STARCH, CORN (UNII: O8232NY3SJ)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColorORANGEScoreno score
ShapeROUNDSize9mm
FlavorImprint Code TCL081
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55154-5889-010 in 1 BAG01/14/201008/31/2020
11 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved drug other01/14/201008/31/2020
Labeler - Cardinal Health (603638201)

Revised: 9/2020
 
Cardinal Health