Home > Pill Identifier > DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet

Pill Identifier Information of DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet

Drug Information

DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet

Imprint: 8
Shape: C48348
Color: C48330
Ingredients: Docusate; sennosides, USP
Size: 8.00
Score: 1
Rxtty: SY
Author: Contract Pharmacy Services-PA
Inactive Ingredients: CARNAUBA WAX / SILICON DIOXIDE / CROSCARMELLOSE SODIUM / DIBASIC CALCIUM PHOSPHATE DIHYDRATE / D&C YELLOW NO. 10 / FD&C YELLOW NO. 6 / HYPROMELLOSE / MAGNESIUM STEARATE / CELLULOSE, MICROCRYSTALLINE / POLYETHYLENE GLYCOL / SODIUM BENZOATE / STEARIC ACID / STARCH, TAPIOCA / TARTARIC ACID / TITANIUM DIOXIDE / ALUMINUM OXIDE>

Complete Information

  • DRUG FACTS

  • ACTIVE INGREDIENT (IN EACH TABLET)

    Docusate sodium 50 mg

    Sennosides 8.6 mg

  • PURPOSE

    Stool softener & Stimulant laxative

  • USES

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

    Do not use
    • this product if you are presently taking mineral oil, unless directed by a doctor
    • laxative products for more than 1 week unless directed by a doctor

    Ask a doctor before use if you have
    • stomach pain
    • nausea
    • vomiting
    • a sudden change in bowel habits that persists over 2 weeks

    Stop use and ask a doctor if you have
    • have rectal bleeding
    • fail to have a bowel movement after the use of a laxative

    These could be signs of a serious condition

    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
    • if you do not have a comfortable bowel movement by the second day, increase dose by one tablet (do not exceed maximum dosage); or decrease dose until you are comfortable
    • agestarting dosemaximum dose
      adults and children 12 years and over2 tablets once a day4 tablets twice a day
      children 6 to under 12 years1 tablet once a day2 tablets twice a day
      children 2 to under 6 years1/2 tablet once a day1 tablet twice a day
      children under 2 yearsask a doctorask a doctor
  • OTHER INFORMATION

    • each tablet contains: calcium 20 mg, sodium 6 mg (LOW SODIUM)
    • TAMPER-EVIDENT: Do not use this product if foil seal on back of blister is cut, torn, broken or missing
    • store at 25°C (77°F) excursions permitted between 15°-30°C (59°-86°F)
  • INACTIVE INGREDIENTS

    carnauba wax, colloidal silicon dioxide, croscarmellose sodium, dibasic calcium phosphate dihydrate, D&C yellow #10 aluminum lake, FD&C yellow #6 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, sodium benzoate, stearic acid, tapioca starch1, tartaric acid1, titanium dioxide

    1may contain these ingredients

  • QUESTIONS OR COMMENTS?

    call 1-888-838-2872, weekdays, 8 AM-5 PM Eastern Time

    Distributed by:
    GOLDLINE LABORATORIES, INC.
    Sellersville, PA 18960 Dist. 1999 0110REV 89
    192B R1009

    Repackaged by:

    Contract Pharmacy Services-PA
    125 Titus Ave Suite 200
    Warrington, PA 18976 USA

    Original--08/2010--NJW

  • Package Label

    Blister of 30 Tablets

  • INGREDIENTS AND APPEARANCE
    SENNA-S 
    docusate sodium and sennosides tablet, film coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67046-670(NDC:0182-1113)
    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
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    HYPROMELLOSE (UNII: 3NXW29V3WO)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    STARCH, TAPIOCA (UNII: 24SC3U704I)  
    TARTARIC ACID (UNII: W4888I119H)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    Product Characteristics
    ColorYELLOWScoreno score
    ShapeROUNDSize8mm
    FlavorImprint Code 8
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67046-670-3030 in 1 BLISTER PACK
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart33408/17/2010
    Labeler - Contract Pharmacy Services-PA (945429777)
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