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Colistat

Medically reviewed by Drugs.com. Last updated on Jul 6, 2021.

Dosage form: tablet, film coated
Ingredients: DOCUSATE SODIUM 100mg
Labeler: Amvilab LLC
NDC Code: 69975-750

Drug Facts

Active ingredient (in each tablet)

Docusate Sodium 100 mg

Purpose

Stool Softener

Uses
  • for relief of occasional constipation (irregularity).This product generally produces a bowel movement within 12 to 72 hours.

Warnings

Do not use
  • laxative products for longer than one week unless directed to do so by a doctor
  • if you are presently taking mineral oil unless told to do so by a doctor

Ask a doctor before use if you have
  • stomach pain
  • nausea
  • vomiting
  • noticed  a sudden change in bowel habits that lasts over 2 weeks

Stop use and ask a doctor if
  • you have rectal bleeding
  • you fail to have a bowel movement after use

These could be signs of a serious condition.


If pregnant or breast-feeding,

ask a doctor before use.

Keep out of Reach of Children.

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

Directions
Adults and
children 12 years of age and older:
Take 1 tablet as needed,
not to exceed more than 3
tablets daily, or as directed
by a doctor.
Children under
12 years of age:
Consult a doctor before use.






Other information
  • Each tablet contains: Calcium 40 mg
  • Each tablet contains: Sodium 10  mg
  • Store at room temperature.
  • Do not use if imprinted safety seal is broken or missing

Inactive ingredients

Croscarmellose Sodium, Dicalcium Phosphate, Hypromellose, Magnesium Stearate, Microcrystalline Cellulose, Polyethylene Glycol, Pregelatinized Starch, Silica, Sodium Benzoate, Stearic Acid.

Questions?

If you have any questions or comments, or to report an adverse event, please contact +1 404 256 8817

Principal Display Panel

COLISTAT

Docusate Sodium

Stool Softener



  • Gentle
  • Effective
  • Stimulant Free

50 TABLETS 100 mg each




COLISTAT 
docusate sodium tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69975-750
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DOCUSATE SODIUM (DOCUSATE) DOCUSATE SODIUM100 mg
Inactive Ingredients
Ingredient NameStrength
CROSCARMELLOSE SODIUM 
CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE 
HYPROMELLOSES 
MAGNESIUM STEARATE 
CELLULOSE, MICROCRYSTALLINE 
POLYETHYLENE GLYCOLS 
STARCH, CORN 
SILICON DIOXIDE 
SODIUM BENZOATE 
STEARIC ACID 
Product Characteristics
ColorwhiteScore2 pieces
ShapeROUND (Round Biconvex with bisect) Size11mm
FlavorImprint CodeGPI;S1
Contains    
Packaging
#Item CodePackage Description
1NDC:69975-750-0550 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33407/16/2015
Labeler - Amvilab LLC (006092439)
Registrant - Gemini Pharmaceuticals, Inc. dba Plus Pharma (055942270)
Establishment
NameAddressID/FEIOperations
Gemini Pharmaceuticals, Inc. dba Plus Pharma055942270manufacture(69975-750)

 
Amvilab LLC

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.