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

DocQLace

Qualitest Pharmaceuticals

  • 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 Syrup

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredient (in each 15 mL (1 tablespoonful)) :Docusate sodium 60 mg

Purpose

Purpose: Stool Softener

Uses

  • for gentle, reliable relief from occasional constipation (irregularity)
  • generally produces bowel movement in 12 to 72 hours

Warnings

Do not use
  • laxative products for longer than 1 week unless told to do so by a doctor
  • if you are presently taking mineral oil unless told to do so by a doctor
Ask a doctor before use if you have
  • stomach pain
  • nausea
  • vomiting
  • noticed a sudden change in bowel habits that last over two weeks
Stop use and ask a doctor if you have

If pregnant or breast-feeding
Keep out of reach of children

Directions

  • take as directed by a doctor
  • doses must be given in a 6 to 8 oz glass of milk or fruit juice, to prevent throat irritation
  • take only by mouth. Dose may be taken as a single daily dose or in divided doses.
  • dosage should be adjusted to individual response
adults and children 12 years of age and older
1 to 6 tablespoonfuls, or as directed by a doctor
children 6 to under 12 years of age
1 to 2 1/2 tablespoonfuls, or as directed by a doctor
children under 6 years
Ask a doctor
Other information

  • Store at room temperature 20° -25°C.
  • Protect from freezing and excessive heat



Inactive ingredients

alcohol (not more than 1%), citric acid, D&C red no. 33, FD&C red no.40, peppermint flavor, glycerin, methylparaben, propylene glycol, propylparaben, purified water, sodium benzoate, sodium citrate, sucrose.

Qualitest Pharmaceuticals
Huntsville, AL 35811 USA

DocQLace

Docusate sodium SYRUP

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0603-0747
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
DOCUSATE SODIUM DOCUSATE 20 mg

Inactive Ingredients

Ingredient Name Strength
ANHYDROUS CITRIC ACID
D&C RED NO. 33
METHYLPARABEN
propylene glycol
PROPYLPARABEN
SODIUM CITRATE
water
SODIUM BENZOATE
SUCROSE
FD&C RED NO. 40
ALCOHOL
GLYCERIN

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0603-0747-58 473 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part334 1990-10-05


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Be sure to consult your doctor before taking any medication!
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