Label: BISACODYL tablet, coated
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Contains inactivated NDC Code(s)
NDC Code(s): 70518-1864-0, 70518-1864-1 - Packager: REMEDYREPACK INC.
- This is a repackaged label.
- Source NDC Code(s): 0904-6748
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated March 15, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Uses
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Warnings
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
When using this product
- do not chew or crush tablet(s)
- do not use within 1 hour after taking an antacid or milk
- you may have stomach discomfort, faintness and cramps
- stomach pain, nausea or vomiting
- Directions
- Other information
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Inactive ingredients
acacia, ammonium hydroxide, calcium carbonate, carnauba wax, colloidal anhydrous silica, corn starch, D&C yellow #10 aluminum lake, FD&C yellow #6 aluminum lake, hypromellose, iron oxide black, lactose anhydrous, magnesium stearate, methylparaben, polydextrose, polyethylene glycol, polyvinyl acetate phthalate, povidone, propylene glycol, propylparaben, shellac glaze, simethicone, sodium alginate, sodium benzoate, sodium bicarbonate, stearic acid, sucrose, talc, titanium dioxide, triacetin, triethyl citrate
- Questions or comments?
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PRINCIPAL DISPLAY PANEL
DRUG: Bisacodyl
GENERIC: Bisacodyl
DOSAGE: TABLET, COATED
ADMINSTRATION: ORAL
NDC: 70518-1864-0
NDC: 70518-1864-1
COLOR: orange
SHAPE: ROUND
SCORE: No score
SIZE: 6 mm
IMPRINT: 5
PACKAGING: 30 in 1 BLISTER PACK
PACKAGING: 30 in 1 BLISTER PACK
ACTIVE INGREDIENT(S):
- BISACODYL 5mg in 1
INACTIVE INGREDIENT(S):
- POVIDONE, UNSPECIFIED
- TRIACETIN
- TITANIUM DIOXIDE
- TALC
- SUCROSE
- STEARIC ACID
- SODIUM BICARBONATE
- SODIUM BENZOATE
- SODIUM ALGINATE
- WATER
- DIMETHICONE
- SHELLAC
- PROPYLPARABEN
- PROPYLENE GLYCOL
- TRIETHYL CITRATE
- AMMONIA
- POLYETHYLENE GLYCOL, UNSPECIFIED
- POLYDEXTROSE
- METHYLPARABEN
- MAGNESIUM STEARATE
- ANHYDROUS LACTOSE
- FERROSOFERRIC OXIDE
- HYPROMELLOSE, UNSPECIFIED
- FD&C YELLOW NO. 6
- D&C YELLOW NO. 10 ALUMINUM LAKE
- STARCH, CORN
- SILICON DIOXIDE
- CARNAUBA WAX
- CALCIUM CARBONATE
- Polyvinyl Acetate Phthalate
- ACACIA
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INGREDIENTS AND APPEARANCE
BISACODYL
bisacodyl tablet, coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70518-1864(NDC:0904-6748) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BISACODYL (UNII: 10X0709Y6I) (DEACETYLBISACODYL - UNII:R09078E41Y) BISACODYL 5 mg Inactive Ingredients Ingredient Name Strength ACACIA (UNII: 5C5403N26O) CALCIUM CARBONATE (UNII: H0G9379FGK) CARNAUBA WAX (UNII: R12CBM0EIZ) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STARCH, CORN (UNII: O8232NY3SJ) D&C YELLOW NO. 10 ALUMINUM LAKE (UNII: CQ3XH3DET6) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) FERROSOFERRIC OXIDE (UNII: XM0M87F357) ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK) MAGNESIUM STEARATE (UNII: 70097M6I30) METHYLPARABEN (UNII: A2I8C7HI9T) POLYDEXTROSE (UNII: VH2XOU12IE) POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A) POLYVINYL ACETATE PHTHALATE (UNII: 58QVG85GW3) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PROPYLPARABEN (UNII: Z8IX2SC1OH) SHELLAC (UNII: 46N107B71O) DIMETHICONE (UNII: 92RU3N3Y1O) WATER (UNII: 059QF0KO0R) SODIUM ALGINATE (UNII: C269C4G2ZQ) SODIUM BENZOATE (UNII: OJ245FE5EU) SODIUM BICARBONATE (UNII: 8MDF5V39QO) STEARIC ACID (UNII: 4ELV7Z65AP) SUCROSE (UNII: C151H8M554) TALC (UNII: 7SEV7J4R1U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) TRIACETIN (UNII: XHX3C3X673) TRIETHYL CITRATE (UNII: 8Z96QXD6UM) AMMONIA (UNII: 5138Q19F1X) Product Characteristics Color orange Score no score Shape ROUND Size 6mm Flavor Imprint Code 5 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70518-1864-0 30 in 1 BLISTER PACK; Type 0: Not a Combination Product 02/13/2019 2 NDC:70518-1864-1 30 in 1 BLISTER PACK; Type 0: Not a Combination Product 05/28/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 02/13/2019 Labeler - REMEDYREPACK INC. (829572556)