Label: BISACODYL LAXATIVE- bisacodyl suppository
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Contains inactivated NDC Code(s)
NDC Code(s): 49614-133-35 - Packager: Medicine Shoppe International Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 12, 2010
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT (in each suppository)
- PURPOSE
- USES
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WARNINGS
For rectal use only. May cause abdominal discomfort, faintness, rectal burning, and mild cramps.
Do not use
- more than one per day
- for a period of longer than one week unless directed by a doctor
- laxative products when abdominal pain, nausea, or vomiting are present unless directed by a doctor
- if seal under product lid is torn, damaged, or open
Ask a doctor before use
- if you have noticed a sudden change in bowel habits that persist over a period of two weeks
- if you are pregnant or nursing a baby
- DIRECTIONS
- SPL UNCLASSIFIED SECTION
- OTHER INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
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PACKAGE INFORMATION
The Medicine Shoppe®
COMPARE TO ACTIVE INGREDIENT OF DULCOLAX®*
NDC 49614-133-35Gentle Laxative
BISACODYL SUPPOSITORIES
CONSTIPATION RELIEF
8 SUPPOSITORIES 10 MG EACH
FOR YOUR SAFETY, SUPPOSITORIES ARE PACKAGED IN PAMPER-EVIDENT SEALED PLASTIC WRAPPER. DO NOT USE IF PLASTIC WRAPPER IS TORN OR OPEN.
*This product is not manufactured or distributed by Boehringer Ingelhem
Pharmaceuticals, Inc., owner of the registered trademark Dulcolax®.Another Quality Product
Distributed by Medicine Shoppe Int'l., Inc.
St. Louis, MO 63132
www.medicineshoppe.com
A Cardinal Health Company
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INGREDIENTS AND APPEARANCE
BISACODYL LAXATIVE
bisacodyl suppositoryProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49614-133 Route of Administration RECTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength bisacodyl (UNII: 10X0709Y6I) (bisacodyl - UNII:10X0709Y6I) bisacodyl 10 mg Inactive Ingredients Ingredient Name Strength fat, hard (UNII: 8334LX7S21) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49614-133-35 8 in 1 BOX Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part334 03/08/2008 Labeler - Medicine Shoppe International Inc (071997654)