Label: BISACODYL suppository
- NDC Code(s): 82568-0028-2, 82568-0028-5
- Packager: AARNA USA INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 22, 2026
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients (per suppository)
- Purpose
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Warnings
- Do not use laxative products
- Ask a doctor before use if you have
- When using this product
- Stop use and ask a doctor if
- If pregnant or breast-feeding
- Directions
- Other information
- Inactive ingredient
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
BISACODYL
bisacodyl suppositoryProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82568-0028 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 HYDROGENATED PALM KERNEL OIL (UNII: FM8D1RE2VP) Product Characteristics Color white (WHITE TO OFF WHITE) Score Shape OVAL (TORPEDO SHAPE) Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82568-0028-2 12 in 1 BOX 04/21/2026 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:82568-0028-5 50 in 1 BOX 04/21/2026 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 Drug M007 04/21/2026 Labeler - AARNA USA INC. (118515992)


