Label: SENNA-S- docusate sodium, sennosides tablet, film coated

  • NDC Code(s): 63561-0187-2
  • Packager: Granulation Technology, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 26, 2024

If you are a consumer or patient please visit this version.

  • Drug Facts

  • Active ingredients (in each tablet)

    Docusate Sodium         50 mg

    Sennosides                        8.6 mg

  • Purpose

    Stool softener

    Laxative

  • Uses

    • Relieves occasional constipation (irregularity)
    • Generally produces a bowel movement in 6-12 hours
  • Warnings

  • Do not use

    • If you are now taking mineral oil, unless directed by a doctor
    • Laxative products for longer than 1 week unless directed by a doctor
  • Ask a doctor before use if you have

    • Stomach pain
    • Nausea
    • Vomiting
    • Noticed a sudden change in bowel habits that continues over a period of 2 weeks
  • Stop using and ask a doctor if

    you have rectal bleeding or fail to have a bowel movement after use of a laxative. These may indicate 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 (1-800-222-1222) right away.

  • Directions

    • Take preferably at bedtime or as directed by a doctor
    agestarting dosagemaximum dosage
    adults and children
    12 years of age and over
    2 tablets once a day4 tablets twice a day
    children 6 to under 12 years1 tablet once a day2 tablets twice a day
    children 2 to under 6 years1/2 tablet once a day1 tablet twice a day
    children under 2 yearsask a doctorask a doctor

  • Other information

    • Each tablet contains: Calcium 30 mg, Sodium 6 mg LOW SODIUM
    • Store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F)
  • Inactive ingredients

    croscarmellose sodium,dibasic calcium phosphate dihydrate, microcrystalline cellulose, pregelatinized starch, colloidal silicon dioxide, magnesium stearate, polyvinyl alcohol, titanium dioxide, polyethylene glycol (PEG) 3350, talc, FD&C red 40 lake, FD&C yellow 5 lake

  • Principal Display Panel

    NDC 63561-0187-2

    Senna-S

    DOCUSATE SODIUM 50 mg / STOOL SOFTENER

    SENNOSIDES 8.6 mg / LAXATIVE

    Compare to Senokot-S ®Dual Action Active Ingredients

    220 Film-Coated Tablets

    Docusate Sodium 50 mg Sennosides 8.6 mg

    Docusate Sodium 50 mg Sennosides 8.6 mg_peel

  • INGREDIENTS AND APPEARANCE
    SENNA-S 
    docusate sodium, sennosides tablet, film coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63561-0187
    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)  
    DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)  
    MICROCRYSTALLINE CELLULOSE 200 (UNII: 5XDI2TS1EZ)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POLYVINYL ALCOHOL (UNII: 532B59J990)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)  
    TALC (UNII: 7SEV7J4R1U)  
    FD&C RED NO. 40 ALUMINUM LAKE (UNII: 6T47AS764T)  
    FD&C YELLOW NO. 5 ALUMINUM LAKE (UNII: JQ6BLH9FR7)  
    Product Characteristics
    ColororangeScoreno score
    ShapeROUNDSize10mm
    FlavorImprint Code G187
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63561-0187-2220 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/26/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)11/26/2024
    Labeler - Granulation Technology, Inc. (847132193)
    Registrant - Granulation Technology, Inc. (847132193)
    Establishment
    NameAddressID/FEIBusiness Operations
    Granulation Technology, Inc.847132193manufacture(63561-0187)