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

Active ingredient

Drug Facts

Active Ingredient (in each tablet)

Standardized senna concentrate, sennosides 8.6 mg

Docusate sodium 50 mg

Purpose

Stimulant Laxative

Stool Softener

Uses

Provides relief of simple constipation by softening hard, dry stools and gentle bowel stimulating action. Generally produces a bowel movement within 6 to 12 hours.

Warnings

Ask a doctor before use if you have nausea, vomiting, abdominal pain, or sudden change in bowel habits that persist over a period of 2 weeks

When using this product do not use for more than 7 days unless directed by a doctor

Stop use and ask a doctor if rectal bleeding or failure to have a bowel movement occurs after the use of a laxative. These could be signs of a serious condition.

This product 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

Recommended dosage (or as directed by a doctor): Take preferably at bedtime.

age

starting dose

maximum dose

adults and children 12 years & over

2 tablets once a day

4 tablets twice a day

6 to under 12 years

1 tablet once a day

2 tablets twice a day

2 to under 6 years

1/2 tablet once a day

1 tablet twice a day

under 2 years

consult a doctor

Inactive ingredients

Croscarmellose Sodium, Dicalcium Phosphate, FD&C Yellow #5 Lake**, FD&C Yellow #6 Lake, Hydroxypropylmethylcellulose, Magensium Silicate, Magnesium Stearate, Microcrystalline Cellulose, Mineral Oil, Polyethylene Glycol, Sodium Benzoate, Sodium Lauryl Sulfate, Starch, Stearic Acid and Titanium Dioxide.

Storage

Store at Controlled Room Temperature between 15-30 C (59-86F)

Questions?

Adverse Drug Event

Call: (800) 616-2471

Other Information

**Warning: Contains FD&C Yellow #5 Lake (Tartrazine) as a color additive.

Distributed by

Major Pharmaceuticals

31778 Enterprise Drive

Livonia, MI 48150 USA

MFGD By
Contract Pharma.,
NY 11788

Senna Plus Tablets 8.6/50 MG

Standardized Senna Concentrate & Docusate Sodium 10 Tablets

Repackaged by Cardinal Health

Zanesville, OH 43701

L4121711-11212

L4121711-21212

Package/Label Principal Display Panel

Senna Plus Tablets 8.6/50 mg

Standardized Senna Concentrate

& Docusate Sodium

10 Tablets

bag label

Package/Label 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:55154-0743(NDC:0904-5512)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES8.6 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
ShapeROUNDSize10mm
FlavorImprint Code CPC;490
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55154-0743-010 in 1 BAG01/14/201010/31/2014
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 other01/14/201010/31/2014
Labeler - Cardinal Health (188557102)
Establishment
NameAddressID/FEIBusiness Operations
Cardinal Health188557102REPACK(55154-0743)

Revised: 6/2017
 
Cardinal Health