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

DocQLace

State of Florida DOH Central Pharmacy

  • 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
DocQLace

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Docusate sodium 100 mg

Stool softener

  • relieves occasional constipation (irregularity)  
  • generally produces bowel movement in 12 to 72 hours

Do not use if you are presently taking mineral oil, unless told to do so by a doctor

  • stomach pain  
  • nausea  
  • vomiting  
  • noticed a sudden change in bowel habits that lasts over 2 weeks
  • you have rectal bleeding or fail to have a bowel movement after use of a laxative. 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.

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

doses may be taken as a single daily dose or in divided doses

adults and children 12 years and over  take 1-3 softgels daily 
children 2 to under 12 years of age  take 1 softgel daily 
children under 2 years  ask a doctor 
  • each softgel contains: sodium 5 mg VERY LOW SODIUM  
  • store at 15°-30°C (59°-86°F)  
  • keep tightly closed

You may report serious side effects to: 130 Vintage Drive, Huntsville, AL 35811.

FD&C Red #40, FD&C Yellow #6, gelatin, glycerin, polyethylene glycol 400, purified water, sorbital special

Manufactured for:
QUALITEST PHARMACEUTICALS
HUNTSVILLE, AL 35811

They are supplied by State of Florida DOH Central Pharmacy as follows:

NDC Strength Quantity/Form Color Source Prod. Code
53808-0677-1 100 mg 30 Capsules in a Blister Pack Reddish 0603-0150

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL 

DocQLace

docusate sodium CAPSULE

Product Information

Product Type Human otc drug label Item Code (Source) NDC:53808-0677(NDC:0603-0150)
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 400
water
sorbitol

Product Characteristics

Color Size Imprint Code Shape
RED (Reddish) 12 mm SCU1 CAPSULE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:53808-0677-1 30 in 1 BLISTER PACK

Marketing Information

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


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.