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Stool Softener

EQUALINE (SuperValu)
P and L Development of New York Corporation

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Docusate Sodium 100 mg

Stool softener

  • temporary relief of occasional constipation
  • this product generally produces a bowel movement within 12 to 72 hours.
  • if abdominal pain, nausea or vomiting are present
  • you notice a sudden change in bowel habits that persists over a period of 2 weeks
  • you are presently taking mineral oil
  • rectal bleeding or failure to have a bowel movement occur after use which may indicate a serious condition
  • you need to use a laxative for more than 1 week

ask a health care professional before use.

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

  • take with a glass of water
adults and children 12 years of age and over take 1 to 3 softgels daily. This dose may be taken as a single daily dose or in divided doses.
children 2 to under 12 years of age  take 1 softgel daily
children under 2 years of age  ask a doctor
  • each softgel contains: sodium 6 mg
  • store at controlled room temperature 15o - 30o C (59o- 86o F)

edible ink, FD&C Red #40, FD&C Yellow #6, gelatin, glycerin, polyethylene glycol, propylene glycol, purified water, sorbitol special.

Questions or Comments ?

Call 1-877-932-7948

Principal Display Panel

Compare to Dulcolax® Stool Softener*

easy & gentle

stool softener

Docusate sodium 100 mg

fast, dependable relief of occasional constipation

  • predictable releif
  • easy to swallow softgels
  • safe & effective without harsh laxatives

DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.

*This product is not manufactured or distributed by Boehringer Ingelheim Consumer Healthcare owner of the registered trademark of Dulcolax®

Stool Softener
Docusate Sodium 100 mg softgels

Stool Softener

DOCUSATE SODIUM CAPSULE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:41163-006
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 GLYCOLS
propylene glycol
water
sorbitol

Product Characteristics

Color Size Imprint Code Shape
ORANGE 13 mm P51 OVAL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 25 in 1 BOTTLE
2 NDC:41163-006-25 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part334 2013-04-04


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