DULCOLAX - bisacodyl suppository 
Boehringer Ingelheim Pharmaceuticals, Inc.

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Dulcolax® Suppository

Drug Facts

Active ingredient (in each suppository) Purpose
Bisacodyl USP 10 mg .................................... Stimulant laxative

Uses

Warnings

For rectal use only

Ask a doctor before use if you have

When using this product it may cause stomach discomfort, faintness, rectal burning and mild cramps

Stop use and ask a doctor if

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

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 years of age 1/2 suppository in a single daily dose
children under 2 years of age ask a doctor

Other information

Inactive ingredient

hydrogenated vegetable oil

Dulcolax Suppository Carton

DULCOLAX 
bisacodyl   suppository
Product Information
Product Type HUMAN OTC DRUG NDC Product Code (Source) 0597-0052
Route of Administration RECTAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
bisacodyl (bisacodyl) bisacodyl 10 mg
Inactive Ingredients
Ingredient Name Strength
No Inactive Ingredients Found
Product Characteristics
Color WHITE Score     
Shape BULLET Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0597-0052-16 4 BLISTER PACK In 1 CARTON contains a BLISTER PACK
1 4 SUPPOSITORY In 1 BLISTER PACK This package is contained within the CARTON (0597-0052-16)
2 0597-0052-28 7 BLISTER PACK In 1 CARTON contains a BLISTER PACK
2 4 SUPPOSITORY In 1 BLISTER PACK This package is contained within the CARTON (0597-0052-28)
3 0597-0052-34 1 BLISTER PACK In 1 CARTON contains a BLISTER PACK
3 4 SUPPOSITORY In 1 BLISTER PACK This package is contained within the CARTON (0597-0052-34)
4 0597-0052-38 2 BLISTER PACK In 1 CARTON contains a BLISTER PACK
4 4 SUPPOSITORY In 1 BLISTER PACK This package is contained within the CARTON (0597-0052-38)
5 0597-0052-44 1 BLISTER PACK In 1 CARTON contains a BLISTER PACK
5 1 SUPPOSITORY In 1 BLISTER PACK This package is contained within the CARTON (0597-0052-44)

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part334 04/01/2002

Labeler - Boehringer Ingelheim Pharmaceuticals, Inc. (603175944)
Establishment
Name Address ID/FEI Operations
Istituto De Angeli S.r.l. 436912369 MANUFACTURE
Revised: 11/2010 Boehringer Ingelheim Pharmaceuticals, Inc.