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
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated March 1, 2023

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 product you 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 ingredient hard 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 not finalpart33412/16/2018
    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)