Label: SENNA- sennosides tablet

  • NDC Code(s): 71399-1017-1, 71399-1017-2, 71399-1017-3
  • Packager: Akron Pharma Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 18, 2023

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  • Drug Facts

    Active ingredient (in each tablet)

    Sennosides 8.6 mg

  • Purpose

    Laxative

  • Uses

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

    Do not use

    • laxative products for longer than one week unless directed by a doctor

    Do not use

    laxative products for longer than one 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 breast-feeding,

    ask a health care 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

    agestarting dosagemaximum 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 of age

    1 tablet

    once a day

    2 tablets

    twice a day

    Children 2 to under

    6 years of age

    1/2 tablet

    once a day

    1 tablet

    twice a day

    Children under

    2 years of age

    ask a doctor

    ask a doctor

  • Other information

    • Each tablet contains: Calcium 14 mg
    • Store between 15º to 30ºC (59 to 86F)
  • Inactive ingredients

    microcrystaline cellulose, dicalcium phosphate, sodium starch glycolate, croscarmellose sodium, hypromellose, povidone, collodial silicon dioxide, megnesium stearate. 

  • Questions or comments?

    1-(877) 255-6999

  • SPL UNCLASSIFIED SECTION

    Tamper Evident:

    Do not use if imprinted inner safety seal is torn or missing.

    This product is not manufactured or distributed by Purdue Products L.P.,

    Owner of the registered trademark Senokot®

    Manufactured for:

    Akron Pharma Inc

    Fairfield, NJ 07004

    www.akronpharma.com

  • PRINCIPAL DISPLAY PANEL

    100

    100UD

    1000

  • INGREDIENTS AND APPEARANCE
    SENNA 
    sennosides tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71399-1017
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SENNOSIDES (UNII: 3FYP5M0IJX) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES8.6 mg
    Inactive Ingredients
    Ingredient NameStrength
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    POVIDONE (UNII: FZ989GH94E)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TALC (UNII: 7SEV7J4R1U)  
    Product Characteristics
    ColorbrownScoreno score
    ShapeROUNDSize3mm
    FlavorImprint Code 86;A
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71399-1017-1100 in 1 BOTTLE; Type 0: Not a Combination Product12/06/2024
    2NDC:71399-1017-21000 in 1 BOTTLE; Type 0: Not a Combination Product12/06/2024
    3NDC:71399-1017-3100 in 1 PACKAGE12/06/2024
    31 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00712/06/2024
    Labeler - Akron Pharma Inc. (067878881)
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