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

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DulcoEase Pink

Boehringer Ingelheim Pharmaceuticals, Inc.
Boehringer Ingelheim Pharmaceuticals, Inc.




FULL PRESCRIBING INFORMATION

Active ingredient

Drug Facts

Active ingredient (in each softgel) Purpose
Docusate sodium 100mg............................................................................................................................. Stool softener laxative

Purpose

Use

  • for temporary relief of occasional constipation and irregularity
  • this product generally produces bowel movement in 12 to 72 hours

Warnings

Ask a doctor before use if you have

  • stomach pain, nausea or vomiting
  • a sudden change in bowel habits that lasts more than 2 weeks

Stop use and ask a doctor if

  • you have rectal bleeding or no bowel movement after using this product. These could be signs of a serious condition.
  • you need to use a laxative for more than 1 week

If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions take with a glass of water

adults and children 12 years and over 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 1 softgel daily
children under 2 years ask a doctor

Other information

  • each softgel contains: sodium 6mg
  • store at 20–25°C (68-77°F)
  • protect from excessive humidity
  • do not use this product if the safety seal under the cap is torn or missing

Inactive ingredients

D&C Red #33, FD&C Blue #1, FD&C Red #40, FD&C Yellow #6, gelatin, glycerin, hypromellose, iron oxide, polyethylene glycol, propylene glycol, purified water, sorbitan, sorbitol, titanium dioxide

Questions? Call toll-free 1-888-285-9159 (English/Spanish)
Or visit www.DulcolaxUSA.com



Uses

DulcoEase® Pink 25 Capsules
NDC: 0597-0151-23

DulcoEase Pink

DulcoEase Pink

docusate sodium CAPSULE, LIQUID FILLED

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0597-0151
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
D&C RED NO. 33
FD&C BLUE NO. 1
FD&C RED NO. 40
FD&C YELLOW NO. 6
GELATIN
GLYCERIN
HYPROMELLOSES
ferric oxide red
POLYETHYLENE GLYCOLS
propylene glycol
water
sorbitol
SORBITAN
titanium dioxide

Product Characteristics

Color Size Imprint Code Shape
WHITE (white on the other) 13 mm L486 OVAL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 25 in 1 BOTTLE
2 30 in 1 BOTTLE
3 90 in 1 BOTTLE
4 NDC:0597-0151-90 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part334 2013-02-01


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Be sure to consult your doctor before taking any medication!
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