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Doc Q Lace

Dosage form: liquid
Ingredients: Docusate sodium 10mg in 1mL
Labeler: Qualitest Pharmaceuticals
NDC Code: 0603-0746

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Doc Q Lace Liquid

Active Ingredient: Docusate sodium 10 mg (in each mL)

Purpose: Stool Softener

  • 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 rectal bleeding or fail to have a bowel movement after use of a laxative. These could be signs of a serious condition.

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.

  • take as directed by doctor
  • this product must be given in a 6 to 8 oz. glass of milk or fruit juice to prevent throat irritation.  Dose may be taken as a single daily dose or in divided doses
  • dosage should be adjusted to individual response
  • higher doses are recommended for initial therapy
  • the effect on stools is usually apparent 1 to 3 days after the first dose
Adults and children over 12 years of age and older
50 to 200 mg (1 to 4 teaspoonful)
Children 6 to under 12 years of age
50 to 100 mg (1 to 2 teaspoonful)
Children 3 to under 6 years of age
25 to 50 mg(1/2 to 1 teaspoonful)
children under 3 years of age
Ask a doctor
Other information
  • Store at room temperature 20°-25°C (68°-77°F)
  • protect from freezing and excessive heat

Inactive ingredients

citric acid, D&C red no. 33, flavor, methylparaben, Poloxamer, propylene glycol, propylparaben, purified water, sodium citrate.

You may report serious side effects to:

130 Vintage Drive
Huntsville, AL 35811

docusate sodium liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0603-0746
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Docusate sodium (Docusate) Docusate sodium10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
anhydrous citric acid 
D&C red no. 33 
propylene glycol 
sodium citrate 
Poloxamer 407 
Product Characteristics
Color    Score    
FlavorLEMON (Lemon Vanilla Flavor) Imprint Code
#Item CodePackage Description
1NDC:0603-0746-58473 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33410/05/1990
Labeler - Qualitest Pharmaceuticals (011103059)

Revised: 06/2012
Qualitest Pharmaceuticals

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.