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Stool softener plus stimulant laxative - Medication Information

Product NDC Code 70000-0519
Drug Name

Stool softener plus stimulant laxative

Type Brand
Active Ingredients
Docusate sodium 50 mg/1
Sennosides 8.6 mg/1
Route ORAL
Dosage Form TABLET
RxCUI drug identifier 998740
Application Number M007
Labeler Name Cardinal Health
Packages
Package NDC Code Description
70000-0519-1 200 tablet in 1 bottle, plastic (70000-0519-1)
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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 only by mouth. Doses may be taken as a single daily dose, preferably in the evening, or in divided doses adults and children 12 years and over take 2-4 tablets daily children 6 to under 12 years of age take 1-2 tablets daily children 2 to under 6 years of age take up to 1 tablet daily children under 2 ask a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients colloidal silicon dioxide, croscarmellose sodium, dicalcium phosphate, FD&C Red #40, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, purified water, stearic acid, titaniumdioxide

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 (irregularity) ■ generally produces bowel movement in 6-12 hours

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
STOOL SOFTENER PLUS STIMULANT LAXATIVE DOCUSATE SODIUM,SENNOSIDES SILICON DIOXIDE CROSCARMELLOSE SODIUM ANHYDROUS DIBASIC CALCIUM PHOSPHATE FD&C RED NO. 40 HYPROMELLOSE, UNSPECIFIED MAGNESIUM STEARATE MICROCRYSTALLINE CELLULOSE POLYETHYLENE GLYCOL, UNSPECIFIED WATER STEARIC ACID TITANIUM DIOXIDE DOCUSATE SODIUM DOCUSATE SENNOSIDES SENNOSIDES S44

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 image.jpg

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.
Drug Facts Active ingredients (in each tablet) Docusate sodium 50 mg Sennosides 8.6 mg

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 ■ stomach pain ■ nausea ■ vomiting ■ noticed a sudden change in bowel habits that lasts over 2 weeks

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 1-800-222-1222

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Other information ■ each tablet contains: calcium 20 mg, sodium 6 mg ■ store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F)

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions or comments? 1-888-333-9792

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 have rectal bleeding or fail to have a bowel movement after use of a laxative. These could be signs of a serious condition.

Pregnancy or breast feeding

Pregnancy or Breast feeding
If pregnant or breast-feeding, 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 ■ laxative products for longer than 1 week unless directed by a doctor ■ if you are presently taking mineral oil, unless directed by a doctor

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