DocQLace Syrup

Pronunciation

Generic Name: docusate sodium
Dosage Form: oral syrup

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

DocQLace Syrup

Drug Facts

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

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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 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) 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
# Item Code Package Description
1 NDC:0603-0747-58 473 mL in 1 BOTTLE, PLASTIC
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: 06/2010
 
Qualitest Pharmaceuticals



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