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Stool softener - Medication Information

Product NDC Code 57896-421
Drug Name

Stool softener

Type Brand
Active Ingredients
Docusate sodium 100 mg/1
Route ORAL
Dosage Form TABLET
RxCUI drug identifier 1099279
Application Number M007
Labeler Name Geri-Care Pharmaceuticals, Corp
Packages
Package NDC Code Description
57896-421-01 100 tablet in 1 bottle (57896-421-01)
57896-421-10 1000 tablet in 1 bottle (57896-421-10)
57896-421-20 200 tablet in 1 bottle (57896-421-20)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Docusate Sodium 100 mg

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 adults and children 12 years and older: take 1-3 tablets daily, or as directed by a doctor. May be taken as a single daily dose or in divided doses. children under 12: consult a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients cellulose, croscarmellose sodium, dicalcium phosphate, magnesium stearate, sodium benzoate, silica, stearic acid, talc

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 12 to 72 hours

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
STOOL SOFTENER docusate sodium SODIUM BENZOATE STEARIC ACID DOCUSATE SODIUM DOCUSATE CROSCARMELLOSE SODIUM MICROCRYSTALLINE CELLULOSE ANHYDROUS DIBASIC CALCIUM PHOSPHATE MAGNESIUM STEARATE SILICON DIOXIDE TALC GC422

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.
PACKAGE LABEL 1

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 Keep out of the reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

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? 1-800-540-3765

Storage and handling

Information about safe storage and handling of the drug product.
Other information each tablet contains: calcium 50 mg, sodium 8 mg store at room temperature 15°C-30°C (59°F-86°F) Tamper Evident: Do not use if imprinted seal under cap is missing or broken

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 Ask a doctor before use if you have stomach pain, nausea or vomiting have a sudden change in bowel habits that persists over a period of 2 weeks are presently taking mineral oil Stop use and ask a doctor if you need to use a laxative longer than 1 week you have rectal bleeding or fail to have a bowel movement. These could be signs of a serious condition. If pregnant or breast-feeding, ask a health professional before use.

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