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Womens gentle laxative - Medication Information

Product NDC Code 69842-089
Drug Name

Womens gentle laxative

Type Brand
Pharm Class Increased Large Intestinal Motility [PE],
Stimulant Laxative [EPC],
Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
Active Ingredients
Bisacodyl 5 mg/1
Route ORAL
Dosage Form TABLET, COATED
RxCUI drug identifier 308753
Application Number part334
Labeler Name CVS HEALTH CORP
Packages
Package NDC Code Description
69842-089-52 25 tablet, coated in 1 blister pack (69842-089-52)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
ACTIVE INGREDIENT In each tablet: Bisacodyl 5mg In each tablet: Bisacodyl 5mg

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
DOSAGE & ADMINISTRATION adults and children 12 years and over: take 1 to 3 tablets in a single daily dose - children 6 to under 12 years: take 1 tablet in a single daily dose - children under 6 years: ask a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Acadia, Anhydrous Calcium Sulfate, Anhydrous Lactose, Carnauba Wax, Colloidal Silicon Dioxide, Corn Starch, D&C red #27, FD&C blue#2 FD&C yellow #6 aluminum lake, Gelatin, Iron Oxide, Iron Oxide Black, Iron Oxide Yellow(Iron Oxide Ochre), Magnesium Stearate, Microcrystalline Cellulose, Polyethylene Glycol (PEG) 400, Polyvinyl Acetate Phthalates, Povidone, Shellac, Sodium Starch Glycolate, Stearic Acid, Sugar, Talc, Titanium Dioxide

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Uses: relieves occasional constipation and irregularity this product generally produces a bowel movement in 6 to 12 hours

Purpose

Information about the drug product’s indications for use.
PURPOSE Stimulant Laxative Stimulant Laxative

Spl product data elements

Usually a list of ingredients in a drug product.
WOMENS GENTLE LAXATIVE BISACODYL FD&C BLUE NO. 2 MAGNESIUM STEARATE BISACODYL DEACETYLBISACODYL FERRIC OXIDE YELLOW POLYETHYLENE GLYCOL 400 STARCH, CORN GELATIN POLYVINYL ACETATE PHTHALATE SHELLAC STEARIC ACID FERROSOFERRIC OXIDE SUCROSE TALC TITANIUM DIOXIDE POVIDONE ACACIA CALCIUM SULFATE CARNAUBA WAX SILICON DIOXIDE D&C RED NO. 27 ANHYDROUS LACTOSE FD&C YELLOW NO. 6 MICROCRYSTALLINE CELLULOSE SODIUM STARCH GLYCOLATE TYPE A CORN TCL

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
25 CT

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of Reach of Children: In case of overdose, get medical help or contact a Poison Control Center right away.

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warning: Do not use if you cannot swallow without chewing. Ask a doctor before use if you have: stomach pain, nausea or vomiting; A sudden change in bowel habits that lasts more than two weeks. When using this product: Do not chew or crush tablet(s); Do not use within 1 hour after taking an antacid or milk; Do not use this product if you have stomach discomfort, faintness or cramps.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API