Home > Drugs A-Z > Natural Senna

Natural Senna (Contract Pharmacal Corp)

Available Formats

Dosage Form Package Information Links
TABLET 100 TABLET in 1 BOTTLE (10267-1122-1) Label Information
TABLET 1000 TABLET in 1 BOTTLE (10267-1122-4) Label Information

Complete Natural Senna Information

  • SPL UNCLASSIFIED SECTION

    Drug Facts


  • Active ingredient

    (in each rounded tablet)

    Sennosides from Senna Concentrate 8.6 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 one week unless directed by a doctor

  • Ask a doctor before use if you have

    • stomach pain, nausea, or vomiting, noticed a sudden change in bowel habits that continue 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.


  • DOSAGE & ADMINISTRATION

    Directions

    • preferable at bedtime
    • adults – two tablets: maximum of 4 tablets twice daily
    • children (6-12 years) one tablet: maximum 2 tablets twice daily

    Other information

    • Store at room temperature, USP
    • Contains 20 mg of calcium
    • Side effects occur. You may report side effects to FDA at 1-800-FDA-1088 (Toll Free).

  • Inactive ingredient

    Croscarmellose Sodium, Dicalcium Phosphate, Hypromellose, Magnesium Silicate, Magnesium Stearate, Microcrystalline Cellulose, Mineral Oil and Polyethylene Gycol

    *This product is not manufactured or by Purdue Frederick, owner of the registered trademark Senokot®

    Manufactured by:
    Contract Pharmacal Corp.
    135 Adams Avenue
    Hauppauge, NY 11788 USA
    www.cpc.com
      R11/09


  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    f4a8921b-figure-01


  • INGREDIENTS AND APPEARANCE
    NATURAL SENNA 
    sennosides tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:10267-1122
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SENNOSIDES A AND B (UNII: 1B5FPI42EN) (SENNOSIDES - UNII:3FYP5M0IJX) SENNOSIDES A AND B 8.6 mg
    Inactive Ingredients
    Ingredient Name Strength
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    MAGNESIUM SILICATE (UNII: 9B9691B2N9)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    LIGHT MINERAL OIL (UNII: N6K5787QVP)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    Product Characteristics
    Color BROWN (Mottled brown) Score no score
    Shape ROUND Size 9mm
    Flavor Imprint Code 1122
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:10267-1122-1 100 in 1 BOTTLE
    2 NDC:10267-1122-4 1000 in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part334 01/24/2001
    Labeler - Contract Pharmacal Corp (968334974)
    Establishment
    Name Address ID/FEI Business Operations
    Contract Pharmacal Corp 968334974 MANUFACTURE