Label: BISACODYL suppository
- NDC Code(s): 0574-7050-12, 0574-7050-50
- Packager: Padagis US LLC
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated November 15, 2021
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- Official Label (Printer Friendly)
- Active ingredient (in each suppository)
- Purpose
- Use
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Warnings
For rectal use only
Ask a doctor before use if you have
- •
- stomach pain, nausea or vomiting
- •
- a sudden change in bowel habits that lasts more than 2 weeks
- If pregnant or breast-feeding,
- Keep out of reach of children.
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Directions
adults and children 12 years of age and over
1 suppository in a single daily dose. Pull apart foil. Insert suppository well into rectum, pointed end first. Retain about 15 to 20 minutes.
children 6 to under 12 years of age
½ suppository in a single daily dose
children under 6 years of age
ask a doctor
- Other information
- Inactive ingredients
- Questions or comments?
- Package/Label Principal Display Panel
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INGREDIENTS AND APPEARANCE
BISACODYL
bisacodyl suppositoryProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0574-7050 Route of Administration RECTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BISACODYL (UNII: 10X0709Y6I) (DEACETYLBISACODYL - UNII:R09078E41Y) BISACODYL 10 mg Inactive Ingredients Ingredient Name Strength COTTONSEED OIL (UNII: H3E878020N) Product Characteristics Color WHITE (white to cream) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0574-7050-12 12 in 1 CARTON 09/01/1990 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:0574-7050-50 50 in 1 CARTON 09/01/1990 2 1 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 09/01/1990 Labeler - Padagis US LLC (967694121)