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Womens laxative - Medication Information

Product NDC Code 68998-398
Drug Name

Womens 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, DELAYED RELEASE
RxCUI drug identifier 308753
Application Number M007
Labeler Name Marc Glassman, Inc.
Packages
Package NDC Code Description
68998-398-85 1 blister pack in 1 carton (68998-398-85) / 25 tablet, delayed release in 1 blister pack
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Bisacodyl USP 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.
Directions take with water Adults and children 12 years of age and older: take 1 to 3 tablets in a single dose, once daily Children 6 to 12 years of age: take 1 tablet once daily Children under 6 years of age: consult a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients acacia, ammonium hydroxide, calcium carbonate, carnauba wax, colloidal anhydrous silica, corn starch, D&C red #27 aluminum lake, FD&C blue #2 aluminum lake, FD&C yellow # 6 aluminum lake, hypromellose, iron oxide black, lactose anhydrous, magnesium stearate, methylparaben, polyvinyl acetate pthalate, polydextrose, polyethylene glycol, propylparaben, propylene glycol, povidone, shellac glaze, simethicone, sodium alginate, sodium benzoate, sodium bicarbonate, stearic acid, sucrose, talc, titanium dioxide, triacetin, triethyl citrate

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 for relief of occasional constipation and irregularity this product usually causes bowel movements in 6 to 12 hours

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Womens Laxative Bisacodyl BISACODYL DEACETYLBISACODYL ACACIA MAGNESIUM STEARATE POLYETHYLENE GLYCOL 400 POVIDONE SHELLAC STEARIC ACID TALC TITANIUM DIOXIDE TRIACETIN CALCIUM CARBONATE CARNAUBA WAX STARCH, CORN D&C RED NO. 27 FD&C BLUE NO. 2--ALUMINUM LAKE FD&C YELLOW NO. 6 HYPROMELLOSES METHYLPARABEN Polyvinyl Acetate Phthalate POLYDEXTROSE PROPYLENE GLYCOL SODIUM ALGINATE SODIUM BENZOATE SODIUM BICARBONATE SUCROSE TRIETHYL CITRATE 5

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.
Principal Display Panel Women's Laxative Women's Laxative

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Other information store between 68º to 77ºF (20º to 25ºC) do not use if blister unit is broken or torn

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
Ask a doctor before use if you have abdominal pain nausea vomiting notice a sudden change in bowel habits that persists over a period of 2 weeks

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use if you cannot swallow without chewing within 1 hour after taking antacid or milk

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 accidental overdose, get medical help or contact a doctor or Poison Control Center (1-800-222-1222) right away.

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a doctor if you need to use more than 1 week rectal bleeding or failure to have a bowel movement after use of a laxative. These may be signs of a serious condition.

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product do not chew or crush tablets abdominal discomfort, faintness, and cramps may occur

Pregnancy or breast feeding

Pregnancy or Breast feeding
Pregnancy/Breastfeeding ask a health professional before use.

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.
Warnings Do not use if you cannot swallow without chewing within 1 hour after taking antacid or milk Ask a doctor before use if you have abdominal pain nausea vomiting notice a sudden change in bowel habits that persists over a period of 2 weeks When using this product do not chew or crush tablets abdominal discomfort, faintness, and cramps may occur Stop use and ask a doctor if you need to use more than 1 week rectal bleeding or failure to have a bowel movement after use of a laxative. These may be signs of a serious condition. Pregnancy/Breastfeeding ask a health professional before use. Keep out of reach of children In case of accidental overdose, get medical help or contact a doctor or Poison Control Center (1-800-222-1222) right away.

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