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Senna-S by Chain Drug Consortium, LLC

Medically reviewed on January 4, 2018

Dosage form: tablet
Ingredients: SENNOSIDES 8.6mg, DOCUSATE SODIUM 50mg
Labeler: Chain Drug Consortium, LLC
NDC Code: 68016-746

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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Active ingredient (in each tablet)

Docusate Sodium 50 mg
Sennosides 8.6 mg

Purpose

Stool softener

Laxative

Uses
  • relieves occasional constipation (irregularity)
  • this product generally produces a bowel movement in 6 to 12 hours

Warnings

Do not use for more than 1 week unless directed by a doctor

Ask a doctor before use if you

  • have abdominal pain, nausea or vomiting
  • are taking mineral oil
  • have noticed a sudden change in bowel habits that lasts over 2 weeks

Stop use and ask a doctor if you have

  • no bowel movement within 12 hours
  • rectal bleeding
  • these could signs of 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

• do not exceed 8 tablets in 24 hours

Age
Starting Dose
Maximum Dose
adults and children 12 years of age and older
2 tablets once a day preferably at bedtime; increase as needed, or as directed by a doctor
4 tablets in the morning and 4 tablets at bedtime
children under 12 years
ask a doctor

Other information
  • each tablet contains: calcium 20 mg, sodium 6 mg
  • store at room temperature 15° - 30°C (59°-86°F)

Inactive ingredients

cellulose, croscarmellose sodium, dicalcium phosphate, D&C yellow
#10, FD&C yellow #6, hypromellose, magnesium stearate, PEG, silica, sodium benzoate, stearic acid,
titanium dioxide, wax.

Package Label

SENNA-S 
sennosides and docusate sodium tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-746
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SENNOSIDES (SENNOSIDES) SENNOSIDES8.6 mg
DOCUSATE SODIUM (DOCUSATE) DOCUSATE SODIUM50 mg
Inactive Ingredients
Ingredient NameStrength
CELLULOSE, MICROCRYSTALLINE 
CROSCARMELLOSE SODIUM 
CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE 
MAGNESIUM STEARATE 
POLYETHYLENE GLYCOLS 
HYPROMELLOSES 
FD&C YELLOW NO. 6 
SODIUM BENZOATE 
STEARIC ACID 
TITANIUM DIOXIDE 
CARNAUBA WAX 
D&C YELLOW NO. 10 
SILICON DIOXIDE 
Product Characteristics
ColororangeScoreno score
ShapeROUNDSize9mm
FlavorImprint CodeTCL081
Contains    
Packaging
#Item CodePackage Description
1NDC:68016-746-601 BOTTLE in 1 CARTON
160 TABLET in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33405/01/2017
Labeler - Chain Drug Consortium, LLC (101668460)
Registrant - Geri-Care Pharmaceutical Corp (611196254)
Establishment
NameAddressID/FEIOperations
Geri-Care Pharmaceutical Corp611196254repack(68016-746)

 
Chain Drug Consortium, LLC

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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