BISACODYL- bisacodyl suppository

Bisacodyl by

Drug Labeling and Warnings

Bisacodyl by is a Otc medication manufactured, distributed, or labeled by CARDINAL HEALTH, INC., G&W Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT (in each suppository)

Bisacodyl USP, 10 mg

PURPOSE

Laxative

USES

For the relief of occasional constipation. Bowel movement is generally produced in 15 minutes to 1 hour.

WARNINGS

For rectal use only

Do not use
laxative products for a period longer than one week unless directed by a doctor

Ask a doctor before use if you have
abdominal pain, nausea or vomiting
a sudden change in bowel habits that lasts longer than 2 weeks

Stop use and ask a doctor
if rectal bleeding occurs or you fail to have a bowel movement after using a laxative. This may indicate a serious condition.

IF PREGNANT OR BREAST FEEDING,

ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

Remove foil. Insert suppository well into rectum touching the bowel wall. Retain about 15 to 20 minutes.
    
In the presence of anal fissures or hemorrhoids, suppositories should be coated at the tip with petroleum jelly.

OTHER INFORMATION

Store at room temperature

INACTIVE INGREDIENT

hydrogenated vegetable oil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 37205-102-53
LEADER®
BISACODYL SUPPOSITORIES
LAXATIVE
FOR PROMPT RELIEF OF CONSTIPATION
12 BISACODYL SUPPOSITORIES 10 MG EACH
Compare to Dulcolax® active ingredient*
Satisfaction Guaranteed

INGREDIENTS AND APPEARANCE

BISACODYL  
bisacodyl suppository

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37205-102
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
Hydrogenated Palm Kernel Oil (UNII: FM8D1RE2VP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37205-102-53	12 in 1 CARTON

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part334	09/10/1997

Labeler - CARDINAL HEALTH, INC. (097537435)

Registrant - G&W Laboratories, Inc. (001271188)

Establishment
Name	Address	ID/FEI	Business Operations
G&W Laboratories, Inc.		001271188	MANUFACTURE