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BISAC-EVAC

G&W Laboratories, Inc.
G&W Laboratories, Inc.

BISAC-EVAC™Bisacodyl USP 10 mg 


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

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. These may be signs of a serious condition.

IF PREGNANT OR BREAST FEEDING,

ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

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

DIRECTIONS

• see chart below for dose
• remove foil wrapper
• insert suppository well up into the rectum as indicated, and retain it about 15 to 20 minutes

adults and children 12 years and over

1 suppository once daily.

children 6 years to under 12 years

1/2 suppository once daily

children under 6 years

ask a doctor

• 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 0713-0109-08
G&W®
BISAC-EVAC™
Bisacodyl USP LAXATIVE
8 SUPPOSITORIES 10 mg each

BISAC-EVAC

Bisacodyl SUPPOSITORY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0713-0109
Route of Administration RECTAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Bisacodyl Bisacodyl 10 mg

Inactive Ingredients

Ingredient Name Strength
Hydrogenated Palm Kernel Oil

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0713-0109-12 12 in 1 CARTON
2 NDC:0713-0109-01 100 in 1 CARTON
3 NDC:0713-0109-08 8 in 1 CARTON
4 NDC:0713-0109-50 50 in 1 CARTON
5 NDC:0713-0109-05 500 in 1 CARTON
6 NDC:0713-0109-10 1000 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part334 1991-05-22


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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