Colistat

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

Medically reviewed by Drugs.com. Last updated on Jul 6, 2023.

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 Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69975-750
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DOCUSATE SODIUM (DOCUSATE)	DOCUSATE SODIUM	100 mg

Inactive Ingredients
Ingredient Name	Strength
CROSCARMELLOSE SODIUM
CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE
HYPROMELLOSES
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
POLYETHYLENE GLYCOLS
STARCH, CORN
SILICON DIOXIDE
SODIUM BENZOATE
STEARIC ACID

Product Characteristics
Color	white	Score	2 pieces
Shape	ROUND (Round Biconvex with bisect)	Size	11mm
Flavor		Imprint Code	GPI;S1
Contains

Packaging
#	Item Code	Package Description
1	NDC:69975-750-05	50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part334	07/16/2015

Labeler - Amvilab LLC (006092439)

Registrant - Gemini Pharmaceuticals, Inc. dba Plus Pharma (055942270)

Establishment
Name	Address	ID/FEI	Operations
Gemini Pharmaceuticals, Inc. dba Plus Pharma		055942270	manufacture(69975-750)

Document Id: 024105d7-d4a4-4370-acfe-854032e043f5

Set id: 87e4f962-08b8-4817-9c31-d8b411f52af3

Version: 1

Effective Time: 20150716

Amvilab LLC

Further information

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

Medical Disclaimer