DOCQLACE  - docusate sodium syrup 
Qualitest Pharmaceuticals

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DocQLace Syrup

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

Purpose: Stool Softener

Uses

Warnings

Do not use
Ask a doctor before use if you have
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.

Directions

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

You may report serious side effects to:
130 Vintage Drive, Huntsville, AL 35811

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.

Manufactured for:

Qualitest Pharmaceuticals
Huntsville, AL 35811 USA

Container Label


DOCQLACE 
docusate sodium   syrup
Product Information
Product TypeHUMAN OTC DRUGNDC Product Code (Source)0603-0747
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Docusate sodium (Docusate) Docusate sodium20 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
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    
ShapeSize
FlavorPEPPERMINTImprint Code
Contains    
Packaging
#NDCPackage DescriptionMultilevel Packaging
10603-0747-58473 mL In 1 BOTTLE, PLASTICNone

Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33410/05/1990

Labeler - Qualitest Pharmaceuticals (011103059)
Revised: 12/2010Qualitest Pharmaceuticals