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Bisacodyl

Sunrise Pharmaceutical Inc

Bisacodyl USP 5 mg Laxative




FULL PRESCRIBING INFORMATION

Bisacodyl USP 5mg.

Stimulant laxative.

For temporary relief of occasional constipation and irregularity

This product generally produces bowel movement in 6 to 12 hours.

Do not use if you cannot swallow without chewing.

If you have

Stomach pain, nausea or vomiting

A sudden change in bowel habits that lasts for more than 2 weeks.

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.

And ask a doctor if:

You have rectal bleeding or no bowel movement after using this product. These could be signs of serious condition.

You need to use laxative for more than 1 week

Ask a health professional before use.

In case of overdose, get medical help or contact a Poison Control Center right away.

Take with a glass of water

Adults and children 12 years and over 1 to 3 tablets in a single daily dose
Children 6 to under 12 years 1 tablet in a single daily dose
Children under 6 years Ask a doctor

OTHER INFORMATION

Store at 20(-25(C(68(-77(F). Protect from excessive humidity.

Acacia, anhydrous calcium sulfate, anhydrous lactose, carnauba wax, colloidal silicon dioxide, corn starch, D&C yellow #10 Aluminum Lake, FD&C yellow #6 Aluminum Lake, gelatin, iron oxide, iron oxide black, iron oxide yellow, magnesium stearate, microcrystalline cellulose, polyethylene glycol 400, polyvinyl acetate phthalate, povidone, shellac, sodium starch glycolate, stearic acid, sugar, talc, titanium dioxide.

Bisacodyl

Bisacodyl

Bisacodyl TABLET, DELAYED RELEASE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:11534-156
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Bisacodyl Bisacodyl 5 mg

Inactive Ingredients

Ingredient Name Strength
ACACIA
CALCIUM SULFATE ANHYDROUS
ANHYDROUS LACTOSE
carnauba wax
SILICON DIOXIDE
STARCH, CORN
D&C YELLOW NO. 10
FD&C YELLOW NO. 6
GELATIN
FERROSOFERRIC OXIDE
FERRIC OXIDE YELLOW
MAGNESIUM STEARATE
cellulose, microcrystalline
polyethylene glycol 400
povidone
SHELLAC
SODIUM STARCH GLYCOLATE TYPE A POTATO
STEARIC ACID
SUCROSE
talc
titanium dioxide
POLYVINYL ACETATE PHTHALATE

Product Characteristics

Color Size Imprint Code Shape
ORANGE 6 mm TCL;003 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11534-156-01 100 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part334 2005-07-08


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Be sure to consult your doctor before taking any medication!
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