Label: DULCOLAX- bisacodyl tablet, coated
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Contains inactivated NDC Code(s)
NDC Code(s): 54868-0016-0 - Packager: Physicians Total Care, Inc.
- This is a repackaged label.
- Source NDC Code(s): 0597-0012
- 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 November 4, 2011
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- 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)
- it may cause stomach discomfort, faintness and cramps
- do not use within 1 hour after taking an antacid or milk
- Directions
- Other information
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Inactive ingredients
acacia, acetylated monoglyceride, carnauba wax, cellulose acetate phthalate, corn starch, dibutyl phthalate, docusate sodium, gelatin, glycerin, iron oxides, kaolin, lactose, magnesium stearate, methylparaben, pharmaceutical glaze, polyethylene glycol, povidone, propylparaben, Red No. 30 lake, sodium benzoate, sorbitan monooleate, sucrose, talc, titanium dioxide, white wax, Yellow No. 10 lake
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DULCOLAX
bisacodyl tablet, coatedProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54868-0016(NDC:0597-0012) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength bisacodyl (UNII: 10X0709Y6I) (bisacodyl - UNII:10X0709Y6I) bisacodyl 5 mg Inactive Ingredients Ingredient Name Strength acacia (UNII: 5C5403N26O) carnauba wax (UNII: R12CBM0EIZ) cellacefate (UNII: F2O5O2OI9F) starch, corn (UNII: O8232NY3SJ) dibutyl phthalate (UNII: 2286E5R2KE) docusate sodium (UNII: F05Q2T2JA0) gelatin (UNII: 2G86QN327L) glycerin (UNII: PDC6A3C0OX) kaolin (UNII: 24H4NWX5CO) lactose (UNII: J2B2A4N98G) magnesium stearate (UNII: 70097M6I30) methylparaben (UNII: A2I8C7HI9T) shellac (UNII: 46N107B71O) polyethylene glycol (UNII: 3WJQ0SDW1A) povidone (UNII: FZ989GH94E) propylparaben (UNII: Z8IX2SC1OH) sodium benzoate (UNII: OJ245FE5EU) sorbitan monooleate (UNII: 06XEA2VD56) sucrose (UNII: C151H8M554) talc (UNII: 7SEV7J4R1U) titanium dioxide (UNII: 15FIX9V2JP) white wax (UNII: 7G1J5DA97F) Product Characteristics Color ORANGE Score no score Shape ROUND Size 5mm Flavor Imprint Code 12; Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54868-0016-0 1 in 1 CARTON 1 10 in 1 BLISTER PACK Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part334 05/19/2010 Labeler - Physicians Total Care, Inc. (194123980) Establishment Name Address ID/FEI Business Operations Physicians Total Care, Inc. 194123980 relabel