Label: DOCUSATE SODIUM AND SENNOSIDES tablet

  • NDC Code(s): 62993-0002-1, 62993-0002-2, 62993-0002-3, 62993-0002-4, view more
    62993-0002-5
  • Packager: Morepen Laboratories Limited
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 23, 2026

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  • Active Ingredients Label

    Active Ingredient Label

  • Inactive Ingredients Section Label

    Inactive Ingredients Label

  • Purpose Section Label

    Purpose Label

  • Indications & Usage Seciton Label

    Indications & Usage

  • Dosage & Administration Section Label

    Dosage & Administration

  • Questions Section Label

    Questions & Comments

  • Warnings Section Label

    Warnings

    Keep out or Reach of Children Label

    Keep out of Reach of Children

  • Storage and Handling Section Label

    Storage and Handling

  • 30 Tablets Bottle Label (NDC 62993-0002-1)

    Primary Display Panel 30 Tablets

  • 60 Tablets Bottle Label (NDC 62993-0002-2)

    Primary Display Panel 60 Tablets

  • 100 Tablets Bottle Label (NDC 62993-0002-3)

    Primary Display Panel 100 Tablets

  • 1000 Tablets Bottle Label (NDC 62993-0002-4)

    Primary Display Panel 1000 Tablets

  • 3000 Tablets Bottle Label (NDC 62993-0002-5)

    Primary Display Panel 3000 Tablets

  • INGREDIENTS AND APPEARANCE
    DOCUSATE SODIUM AND SENNOSIDES 
    docusate sodium and sennosides tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62993-0002
    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
    CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J)  
    TALC (UNII: 7SEV7J4R1U)  
    POVIDONE K30 (UNII: U725QWY32X)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Product Characteristics
    ColororangeScoreno score
    ShapeROUNDSize10mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62993-0002-130 in 1 BOTTLE; Type 0: Not a Combination Product10/01/2025
    2NDC:62993-0002-260 in 1 BOTTLE; Type 0: Not a Combination Product10/01/2025
    3NDC:62993-0002-3100 in 1 BOTTLE; Type 0: Not a Combination Product10/01/2025
    4NDC:62993-0002-41000 in 1 BOTTLE; Type 0: Not a Combination Product10/01/2025
    5NDC:62993-0002-53000 in 1 BOTTLE; Type 0: Not a Combination Product10/01/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00710/01/2025
    Labeler - Morepen Laboratories Limited (650087067)
    Registrant - Morepen Laboratories Limited (772653251)
    Establishment
    NameAddressID/FEIBusiness Operations
    Morepen Laboratories Limited772653251manufacture(62993-0002) , pack(62993-0002) , analysis(62993-0002) , label(62993-0002)
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