DOC Q LACE  - docusate sodium liquid 
Qualitest Pharmaceuticals

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Doc Q Lace Liquid

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

Purpose: Stool Softener

Uses

• helps soften stool for easy, natural passage
• for constipation due to hard stools
• for maximum ease of stool passage in painful anorectal 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	50 to 200 mg (5-20 mL)
Children 12 to under 6 years	40 to 120 mg (4-12 mL)
Children 3 to under 6 years	20 to 60 mg(2-6 mL)
children under 3 years	Ask a doctor

Higher doses are recommended for initial 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
Shake well before use.
Store at room temperature. Protect from excessive heat.
Dispense in a tight container as described in official compendia.

Inactive ingredients

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

Manufactured for:

Qualitest Pharmaceuticals
130 Vintage Drive
Huntsville, AL 35811
USA

DOC Q LACE  docusate sodium   liquid

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 0603-0746 Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Docusate sodium (Docusate) Docusate sodium 10 mg  in 1 mL

Inactive Ingredients Ingredient Name Strength anhydrous citric acid   D&C red no. 33   methylparaben   propylene glycol   propylparaben   sodium citrate   water   Poloxamer 407

Product Characteristics Color      Score      Shape Size Flavor LEMON (Lemon Vanilla Flavor) Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 0603-0746-58 473 mL In 1 BOTTLE, PLASTIC None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part334	10/05/1990

Labeler - Qualitest Pharmaceuticals (011103059)

Registrant - Silarx Pharmaceuticals, Inc (161630033)

Revised: 12/2010Qualitest Pharmaceuticals