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

DOCUSATE SODIUM

Cypress Pharmaceuticals, Inc.
Cypress Pharmaceuticals, Inc.

  • 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
DOCUSATE SODIUM, USP 100 mg

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient (in each softgel )


Purpose


Uses

  • For the relief of occasional constipation.
  • This product generally produces a bowel movement with in 12 to 72 hours.
  • Helps to prevent dry, hard stools.

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
Stop use and ask a doctor
If pregnant or breast-feeding,
Keep out of reach of children. 

Directions

Adults and Children
over 12 years of age
Take only 1 to 2 softgels preferably at bedtime for 2-3 days or
until bowel movements are normal, or as directed by a doctor.
Children 6 to 12
years of age
Take only 1 softgel preferably at bedtime for 2-3 days or until
bowel movements are normal, or as directed by a doctor.
Children under6
years of age
Do not use this product for children under 6 years of age
unless directed by a doctor.

Other information

  • Each softgel contains 5 mg of Sodium.
  • Store at room temperature between 15°C to 30°C (59° to 86°F).
  • Do not use if safety seal under cap is broken or missing.
  • Keep lid tightly close.
Inactive Ingredients
Questions?





L373
Rev 096/10

Principal Display Panel

Principal Display Panel

DOCUSATE SODIUM

Docusate Sodium CAPSULE, LIQUID FILLED

Product Information

Product Type Human otc drug label Item Code (Source) NDC:60258-955
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
polyethylene glycol
water
sorbitol

Product Characteristics

Color Size Imprint Code Shape
red (Reddish) 12 mm SCU1 OVAL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:60258-955-01 100 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part334 2000-08-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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