Label: CONLAX- bisacodyl suppository

  • NDC Code(s): 72701-102-04, 72701-102-05, 72701-102-08, 72701-102-10, view more
    72701-102-12, 72701-102-16, 72701-102-28, 72701-102-30
  • Packager: Bliss GVS Pharma Limited
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 21, 2024

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient (in each suppository)

    Bisacodyl USP, 10 mg

  • PURPOSE

    Purpose

    Stimulant Laxative

  • INDICATIONS & USAGE

    Use

    • for relief of occasional constipation (irregularity)
    • this product generally produces a bowel movement in 15 minutes to 1 hour
  • WARNINGS

    Warnings

    For rectal use only

  • ASK DOCTOR

    Ask a doctor before use if you have

    • stomach pain, nausea or vomiting
    • a sudden change in bowel habits that lasts more than 2 weeks
  • WHEN USING

    When using this productyou may experience stomach discomfort, faintness, rectal burning and mild cramps

  • STOP USE

    Stop use and ask a doctor if

    • you need to use a laxative product for longer than one week
    • you have rectal bleeding or no bowel movement after using this product. These could be signs of a serious condition.
  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast-feeding,ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions

    adults and children

    12 years of age and over

    1 suppository in a single daily dose. Peel open plastic. Insert suppository

    well into rectum, pointed end first. Retain about 15 to 20 minutes.

    children 6 to under 12 years1/2 suppository in a single daily dose
    children under 6 yearsDo not use

  • STORAGE AND HANDLING

    Other information

    • store at 20-25°C (68-77°F)
    • if suppository softens prior to use, may be placed in refrigerator for short time
  • INACTIVE INGREDIENT

    Inactive ingredienthard fat

  • QUESTIONS

    Questions or Comments?1-888-830-6075

  • OTHER SAFETY INFORMATION

    TAMPER EVIDENT: DO NOT USE IF SEALED WRAPPER AROUND SUPPOSITORIES IS BROKEN OR MISSING

  • SPL UNCLASSIFIED SECTION

    Manufactured and Marketed by:

    BLISS GVS PHARMA LTD.

    102, Hyde Park, Saki Vihar Road,

    Andheri (E), Mumbai - 400 072, INDIA

    Email: info@blissgvs.com

    www.blissgvs.com

  • PRINCIPAL DISPLAY PANEL

    Bliss GVS

    NDC 72701-102-10

    Conlax 10MG

    Bisacodyl USP, 10 mg

    Stimulant Laxative

    Gentle, Predictable, Fast Relief

    10 suppositories

    DO NOT SWALLOW

    CONLAX_Supps(10ct)

  • INGREDIENTS AND APPEARANCE
    CONLAX 
    bisacodyl suppository
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72701-102
    Route of AdministrationRECTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BISACODYL (UNII: 10X0709Y6I) (DEACETYLBISACODYL - UNII:R09078E41Y) BISACODYL10 mg
    Inactive Ingredients
    Ingredient NameStrength
    FAT, HARD (UNII: 8334LX7S21)  
    Product Characteristics
    ColorwhiteScore    
    ShapeBULLETSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72701-102-102 in 1 CARTON12/16/2018
    15 in 1 BLISTER PACK; Type 0: Not a Combination Product
    2NDC:72701-102-0520 in 1 CARTON12/16/2018
    25 in 1 BLISTER PACK; Type 0: Not a Combination Product
    3NDC:72701-102-041 in 1 CARTON12/16/2018
    34 in 1 BLISTER PACK; Type 0: Not a Combination Product
    4NDC:72701-102-082 in 1 CARTON12/16/2018
    44 in 1 BLISTER PACK; Type 0: Not a Combination Product
    5NDC:72701-102-123 in 1 CARTON12/16/2018
    54 in 1 BLISTER PACK; Type 0: Not a Combination Product
    6NDC:72701-102-164 in 1 CARTON12/16/2018
    64 in 1 BLISTER PACK; Type 0: Not a Combination Product
    7NDC:72701-102-287 in 1 CARTON12/16/2018
    74 in 1 BLISTER PACK; Type 0: Not a Combination Product
    8NDC:72701-102-306 in 1 CARTON03/01/2023
    85 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00712/16/2018
    Labeler - Bliss GVS Pharma Limited (675629890)
    Establishment
    NameAddressID/FEIBusiness Operations
    Bliss GVS Pharma Limited675630493manufacture(72701-102) , analysis(72701-102) , label(72701-102) , pack(72701-102)