SENNA-S- senna concentrate/docusate sodium tablet 
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-S

Active ingredient

in each tablet

Docusate Sodium 50 mg

Sennosides 8.6 mg

Purpose

Stool Softener

Laxative

Keep Out of Reach of Children

This unit dose package is not child-resistant. If dispensed for outpatient use, a child-resistant container should be utilized.

Uses

Relieves occasional constipation (irregularity) and generally causes bowel movement in 6 to 12 hours

Warnings

TAMPER EVIDENT: Each tablet is individually sealed. Do not use if blister is torn or broken.

Do not use this product if you are presently taking mineral oil, unless directed by a doctor.

Do not use laxative products for more than 1 week unless directed by a doctor. Ask a doctor before use if you have stomach pain, nausea, vomiting or a sudden change in bowel habits that persists over 2 weeks.

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

If pregnant or breast-feeding, ask a health professional before use. Keep out of the 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) or decrease dose until you are comfortable

age

starting dose

maximum dose

adults and children 12 years and over

2 tablets once a day

4 tablets twice a day

children 6 to under 12 years

1 tablet once a day

2 tablets twice a day

children 2 to under 6 years

1/2 tablet once a day

1 tablet twice a day

children under 2 years

ask a doctor

ask a doctor

Inactive ingredients

Carnauba wax, colloidal silicon dioxide, croscarmellose sodium, dibasic calcium phosphate dihydrate, D&C Yellow #10 aluminum lake, FD&C Yellow #6 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol (PEG) 8000, sodium benzoate, stearic acid, titanium dioxide

Each tablet contains:

calcium 20 mg

sodium 6 mg

LOW SODIUM

Storage: Store at Room Temperature 15-30 (59-86 F)

Questions?

Call 1-888-838-2872, weekdays, 8 AM- 5 PM Eastern Time.

Manufactured for:

Goldline Laboratories, Inc.

a subsidiary of IVAX Pharmaceuticals, Inc.

Miami, FL 33137-3227

by: Time-Cap Labs, Inc. Farmingdale, NY 11735

Repackaged by Cardinal Health

Zanesville, OH 43701

Principal Display Panel

Senna-S Tablets

Natural Vegetable Stimulant Laxative

and Stool Softener

10 Tablets

bag label
SENNA-S 
senna concentrate/docusate sodium tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55154-6151(NDC:0182-8642)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DOCUSATE SODIUM (UNII: F05Q2T2JA0) (DOCUSATE - UNII:M7P27195AG) DOCUSATE SODIUM50 mg
SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES8.6 mg
Inactive Ingredients
Ingredient NameStrength
CARNAUBA WAX (UNII: R12CBM0EIZ)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)  
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColorORANGEScoreno score
ShapeROUNDSize10mm
FlavorImprint Code TCL;081
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55154-6151-010 in 1 BAG06/03/201105/31/2012
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 other06/03/201105/31/2012
Labeler - Cardinal Health (188557102)
Establishment
NameAddressID/FEIBusiness Operations
Cardinal Health188557102REPACK(55154-6151)

Revised: 3/2018
 
Cardinal Health