DOCQLACE  - docusate sodium syrup 
Qualitest Pharmaceuticals

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DocQLace Syrup

Drug Facts

Active ingredient (in each teaspoonful(5 mL))         Purpose

Docusate 20 mg . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Stool Softener

Uses

• helps stool soft for easy, natural passage
• for constipation due to hard stools
• for maximum ease of stool passage in painful anorectal conditions, in cardiac and other conditions
  

Warnings

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

Adults and children over 12 years	1 to 3 tablespoonfuls
Children 12 to under 6 years	2 teaspoonfuls
children under 6 years	Ask a doctor

Higher doses are recommended for initial therapy. Dosage should be adjusted nitial therapy. Dosage should be adjusted to individual response. The effect on stools is usually apparent 1 to 3 days after the first dose. This product must be given in a 6 to 8 oz. glass of milk or fruit juice or infant formula to prevent throat irritation

Other information

Store at room temperature. Protect from freezing.
Dispense in a tight container as described in official compendia.

Inactive ingredients

alcohol(not more than 1%), citric acid, D&C red no. 33, FD&C red no.6, glycerin, flavor, methylparaben, sodium benzoate, propylene glycol, propylparaben, purified water, sodium citrate, sucrose.

Manufactured for:

Qualitest Pharmaceuticals
130 Vintage Drive
Huntsville, AL 35811
USA

DOCQLACE  docusate sodium   syrup

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 0603-0747 Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Docusate sodium (Docusate) Docusate sodium 20 mg  in 5 mL

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

Product Characteristics Color      Score      Shape Size Flavor PEPPERMINT Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0603-0747-58 473 mL In 1 BOTTLE, PLASTIC None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		10/05/1990

Labeler - Qualitest Pharmaceuticals (011103059)

Registrant - Silarx Pharmaceuticals, Inc (161630033)

Revised: 06/2010Qualitest Pharmaceuticals