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

Senna Plus by

Drug Labeling and Warnings

Senna Plus by is a Otc medication manufactured, distributed, or labeled by Cardinal Health. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

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

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55154-5889(NDC:0904-6339)
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	8.6 mg
DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG)	DOCUSATE SODIUM	50 mg

Inactive Ingredients
Ingredient Name	Strength
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
Color	ORANGE	Score	no score
Shape	ROUND	Size	9mm
Flavor		Imprint Code	TCL081
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55154-5889-0	10 in 1 BAG	01/14/2010
1		1 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Unapproved drug other		01/14/2010

Labeler - Cardinal Health (603638201)