Label: SENOKOT- standardized senna concentrate tablet, film coated

  • NDC Code(s): 67618-120-06, 67618-120-12, 67618-120-36, 67618-120-72, view more
    67618-120-73
  • Packager: Atlantis Consumer Healthcare, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated August 20, 2025

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  • Active ingredient (in each tablet)

    Sennosides 17.2 mg

  • Purpose

    Laxative

  • Uses

    • relieves occasional constipation (irregularity)
    • generally causes bowel movement in 6-12 hours
  • Warnings

    Do not use 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 movements that continuesover a period of 2 weeks
  • Stop Use

    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.

  • Pregnancy or Breast Feeding

    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

    • take preferably at bedtime or as directed by a doctor
  • Dosage Forms & Strengths

    agestartingdosagemaximumdosage
    adults and children 12 yearsof age and over1 tablet once a day2 tablets
    twice aday
    children 6 to under 12 years½ tablet once a day1 tablet
    twice aday
    children under 6 ask a doctorask a doctor
  • Other Information

    • each tablet contains: calcium 20mg
    • store at 25°C (75°F); excursions permitted between 15°-30°C (59°-86°F).
  • Inactive Ingredients

    croscarmellose sodium, dicalcium phosphate, hypromellose, lactose, magnesium stearate, microcrystalline cellulose, mineral oil, stearic acid, talc, tartaric acid

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Senokot® Extra Strength
    36 Tablets Carton

    36 Tablets Carton

    Senokot® Extra Strength
    12 Tablets Carton

    Carton 12 Tablets

    Senokot® Extra Strength 36 Tablets Label

    Label 36

    Senokot®
    Standardized Senna Concentrate, 17.2mg
    Extra
    Strength

    Natural vegetable
    laxative Ingredient

    72 Tablets

    DO NOT USE IF SEAL UNDER CAP IS
    MISSING OR DAMAGED.

    A0725

    LOT:

    EXP:

    R54038

    Dist. by: Atlantis Consumer Healthcare Inc.
    Bridgewater, NJ 08807 USA
    Questions? 1-833-288-2684 www.senokot.com
    ©2025 Atlantis Consumer Healthcare Inc.

    72ct front
    72ct rear
  • INGREDIENTS AND APPEARANCE
    SENOKOT 
    standardized senna concentrate tablet, film coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67618-120
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES17.2 mg
    Inactive Ingredients
    Ingredient NameStrength
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    TARTARIC ACID (UNII: W4888I119H)  
    DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)  
    LIGHT MINERAL OIL (UNII: N6K5787QVP)  
    TALC (UNII: 7SEV7J4R1U)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Product Characteristics
    ColorBROWN (Light Brown) Scoreno score
    ShapeROUNDSize9mm
    FlavorImprint Code X
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67618-120-121 in 1 CARTON09/01/1988
    112 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:67618-120-363 in 1 CELLO PACK09/01/198801/01/2023
    212 in 1 BLISTER PACK
    212 in 1 BLISTER PACK; Type 0: Not a Combination Product
    3NDC:67618-120-0636 in 1 BOTTLE; Type 0: Not a Combination Product09/01/1988
    4NDC:67618-120-722 in 1 PACKAGE01/01/2024
    41 in 1 CARTON
    436 in 1 BOTTLE; Type 0: Not a Combination Product
    5NDC:67618-120-7372 in 1 BOTTLE; Type 0: Not a Combination Product11/15/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00709/01/1988
    Labeler - Atlantis Consumer Healthcare, Inc. (118983925)
    Registrant - Atlantis Consumer Healthcare, Inc. (118983925)
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