Label: STOOL SOFTENER PLUS LAXATIVE- docusate sodium, sennosides tablet

  • NDC Code(s): 63868-878-60
  • Packager: QUALITY CHOICE (Chain Drug Marketing Association)
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 1, 2024

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  • Active Ingredients (in each tablet)

    Docusate Sodium 50 mg
    Sennosides 8.6 mg

    Purpose

    Stool softener

    Laxative

  • Purpose

    Stool softener

    laxative

  • Uses

    • relieves occasional constipation (irregularity)
    • generally causes 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 use 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 breastfeeding,

    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

     age

    		 starting dosage maximum dosage
     adults and children 12 years of age and older 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
  • Other information

    • each tablet contains: calcium 30 mg
    • each tablet contains: sodium 6 mg LOW SODIUM
    • store at 25ºC (77º); excursions permitted between 15º-30ºC (59º-86ºF)
  • Inactive Ingredients

    croscarmellose sodium, dibasic calcium phosphate dihydrate, FD&C yellow #6 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, silicon dioxide, talc,  titanium dioxide.

  • Questions or comments?

    call 1-800-935-2362 Monday-Friday 9AM-5PM EST

  • Principal Display Panel

    **Compare to the Active Ingredients in Senokot-S®

    Stool Softener Plus Laxative

    Stool Softener • Laxative

    Docusate Sodium, 50 mg | Sennosides, 8.6 mg
    Provides Gentle Relief of: Occasional Constipation

    Tablets

    †This product is not manufactured or distributed by Avrio Health L.P., distributor of Senokot-S®

    TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP ID BROKEN OR MISSING.

    KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.

    Distributed by C.D.M.A., Inc©

    43157 W. 9 Mile Rd

    Novi, MI 48376-0995

    www.qualitychoice.com

  • Product Label

    Docusate Sodium 50 mg, Sennosides 8.6 mg

    QUALITY CHOICE Stool Softener

  • INGREDIENTS AND APPEARANCE
    STOOL SOFTENER PLUS LAXATIVE 
    docusate sodium, sennosides tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-878
    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
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    TALC (UNII: 7SEV7J4R1U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColororangeScoreno score
    ShapeROUNDSize10mm
    FlavorImprint Code PSD22
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63868-878-601 in 1 BOX10/30/2019
    160 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00710/30/2019
    Labeler - QUALITY CHOICE (Chain Drug Marketing Association) (011920774)
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