DOCU LIQUID
-
docusate sodium liquid
Hi-Tech Pharmacal Co., Inc.
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.
----------
noticed a sudden change in bowel habits that lasts over two weeks.
taking any other drug. Take this product two or more hours before or after other drugs. Laxatives may affect how other drugs work.
D&C Red #33, methylparaben, planifoline, poloxamer 181, polyethylene glycol, propylene glycol, propylparaben, purified water, sodium benzoate. Sodium citrate may be used to adjust pH.
Mon. - Thurs. 9:00 am - 4:30 pm EST,
Fri. 9:00 am - 2:30 pm EST.
Serious side effects associated with use of this product may be reported to this number.
REV. 771:04 07/10
NDC 50383-771-16
DOCU LIQUID
(Docusate Sodium 50 mg/5 mL)
STOOL SOFTENER LAXATIVE
TAMPER EVIDENT: FOR YOUR PROTECTION, THIS BOTTLE HAS A SAFETY SEAL AROUND THE NECK OR UNDER THE CAP.
Hi-Tech Pharmacal Co., Inc.
Amityville, NY 11701
NET CONTENTS ONE PINT (473 mL)
DOCU LIQUID
docusate sodium liquid |
||||||||||||||||||||||||
|
||||||||||||||||||||||||
|
||||||||||||||||||||||||
|
||||||||||||||||||||||||
|
||||||||||||||||||||||||
|
Marketing Information | |||
Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
OTC monograph not final | part334 | 08/01/1997 |
Labeler - Hi-Tech Pharmacal Co., Inc. (101196749) |
Revised: 08/2011 Hi-Tech Pharmacal Co., Inc.