Gentle Stool Softener description, usages, side effects, indications, overdosage, supplying and lots more!

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Gentle Stool Softener

Chain Drug Consortium, LLC (Premier Value)

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.

 adults and children 12 years of age and over  take 1 to 3 softgels daily
 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)
  • do not use if imprinted safety seal under cap is broken or missing.
  • *This product is not manufactured or distributed by Boehringer Ingelheim Consumer Healthcare, owner of the registered trademark of Dulcolax®

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

call toll free 1-877-753-3935

Principal Display Panel

*Compare to the active ingredient in Dulcolax® Stool Softener

GENTLE STOOL SOFTENER

DOCUSATE SODIUM, 100 mg per Softgel

For fast, dependable relief of occasional constipation

DISTRIBUTED BY:

CHAIN DRUG CONSORTIUM, LLC.

BOCA RATON, FL 33431

 Gentle Stool Softener

Docusate sodium 100 mg

Gentle Stool Softener

DOCUSATE SODIUM CAPSULE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68016-192
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, PLASTIC
2 NDC:68016-192-25 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part334 2010-07-08


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Be sure to consult your doctor before taking any medication!
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