Label: BISACODYL- bisacodyl suppository
- NDC Code(s): 69842-816-04, 69842-816-08, 69842-816-16
- Packager: CVS Pharmacy
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 12, 2024
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each suppository)
- Purpose
- Use
-
Warnings
For rectal use only
Do not use unless directed by a doctor
- if abdominal pain, nausea or vomiting are present
- for longer than 1 week
Ask a doctor before use if you have
noticed a sudden change in bowel habits that last over a period 2 weeks
- Directions
- Other information
- Inactive ingredients
- CVS Bisacodyl Suppositories
-
INGREDIENTS AND APPEARANCE
BISACODYL
bisacodyl suppositoryProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-816 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) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-816-04 1 in 1 CARTON 04/14/2021 1 4 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:69842-816-08 2 in 1 CARTON 04/14/2021 2 4 in 1 BLISTER PACK; Type 0: Not a Combination Product 3 NDC:69842-816-16 4 in 1 CARTON 04/14/2021 3 4 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 04/14/2021 Labeler - CVS Pharmacy (062312574) Registrant - DSC Laboratories, Inc. (097807374) Establishment Name Address ID/FEI Business Operations DSC Laboratories, Inc. 097807374 manufacture(69842-816)