DOK description, usages, side effects, indications, overdosage, supplying and lots more!

DOK

Major Pharmaceuticals

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
Drug Facts

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient (in each tablet)

Docusate Sodium 100mg

Purpose

Stool Softener

Uses

  • for prevention of dry, hard stools
  • for relief of occasional constipation.This product generally produces a bowel movement within 12 to 72 hours.

Warnings


Do not use

  • if you are currently taking mineral oil, unless directed by a doctor
  • when abdominal pain, nausea, or vomiting are present
  • for longer than one week unless directed by a doctor

Ask a doctor before use if

  • you notice a sudden change in bowel habits that persists over a period of 2 weeks

Stop use and ask a doctor if

  • you have rectal bleeding
  • you fail to have a bowel movement after use

If pregnant or breast-feeding

ask a healthcare professional before use

Keep out of reach of children

Directions

 Adults and children 12 years of age:  Take 2 softgels, preferably at bedtime
 Children 6 to 12 years of age  Take 1 softgel at bedtime

Other information

  • Each softgel contains:  sodium 5mg
  • Store at 20º - 25ºC (68º - 77ºF); excursions permitted to 15º - 30ºC (59º - 86ºF).  [See USP Controlled Room Temperature]

Inactive ingredients

FD&C red #40, FD&C yellow #6, gelatin, glycerin, polyethylene glycol, propylene glycol, purified water and sorbitol special.

Questions or comments? (800) 616-2471

PRINCIPAL DISPLAY PANEL DOK (DOCUSATE SODIUM) SOFTGELS, USP 100MG

PRINCIPAL DISPLAY PANEL DOK (DOCUSATE SODIUM) SOFTGELS, USP 100MG

 

DOK

DOCUSATE SODIUM TABLET, FILM COATED

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0904-2244
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DOCUSATE SODIUM DOCUSATE 100 mg

Inactive Ingredients

Ingredient Name Strength
FD&C RED NO. 40
FD&C YELLOW NO. 6
GELATIN
GLYCERIN
AMMONIUM LAURETH-5 SULFATE
1-PROPOXY-2-PROPANOL
water
sorbitol

Product Characteristics

Color Size Imprint Code Shape
WHITE 11 mm GPI;S1 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0904-2244-61 100 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part334 2011-04-21


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