Label: BISACODYL suppository

  • 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 January 7, 2016

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

  • Drug Facts

    Active ingredient (in each suppository) Purpose

    Bisacodyl USP 10 mg ................................ Stimulant laxative

  • Uses

    relieves occasional constipation.

    this product generally produces a bowel movement in 15 minutes to 1 hour.

  • Directions

    tear off one suppository from the strip.
    tear and peel the wrapper in downward motion.
    continue tearing downward to almost the full length of the suppository (see illustration at the right)
    gently remove the suppository from the wrapper.
    lie on your side and push suppository. with pointed end first, high into the rectum so it will not slip out
    retain it for 15 to 20 minutes.
    Do not exceed recommended dose
    if suppository seems soft, place in refrigerator for a short time before use
    Adults and children 12 years and over 1 suppository once daily.
    Children under 12 years Ask a doctor.

  • DOSAGE & ADMINISTRATION

    Adults and children 12 years and over 1 suppository once daily.
    Children under 12 years Ask a doctor.

  • WARNINGS

    For rectal use only.

    Do not use when abdominal pain, nausea, or vomiting are present.

    Ask a doctor before use if you have a sudden change in bowel habits that lasts over a period of 2 weeks.

    When using this product you may experience. rectal burning. mild cramps.abdominal discomfort. faintness.

    stop use and ask a doctor if you have rectal bleeding. you fill to have a bowel movement after using a laxative. These may be signs of a serious condition.

    you need to use a laxative for more than one week.

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

  • INACTIVE INGREDIENT

    hydrogenated vegetable oil

  • STORAGE

    store at temperatures below 30'C (86'F)

  • OTC - KEEP OUT OF REACH OF CHILDREN

    If swallowed, get medical help or contact a poison control center right away.

  • PRINCIPAL DISPLAY PANEL

    package label

  • INGREDIENTS AND APPEARANCE
    BISACODYL 
    bisacodyl suppository
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54162-006
    Route of AdministrationRECTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BISACODYL (UNII: 10X0709Y6I) (BISACODYL - UNII:10X0709Y6I) BISACODYL0.01 g  in 2 g
    Inactive Ingredients
    Ingredient NameStrength
    HYDROGENATED SOYBEAN OIL (UNII: A2M91M918C)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54162-006-012 g in 1 BOX, UNIT-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart33407/31/2015
    Labeler - Geritrex LLC (112796248)