Label: DOCUSATE SODIUM capsule, liquid filled
- NDC Code(s): 35916-0440-1
- Packager: Softgel Healthcare Pvt Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 31, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
Active ingredient (in each softgel)
Docusate Sodium USP 100 mg
-
Purpose
Stool softener
-
Uses
relieves occasional constipation (irregularity) generally produces bowel movement in 12 to 72 hours
-
Warnings
Do not use - if you are presently taking mineral oil, unless told to do so by a doctor
-
Ask a doctor before use if you have
stomach pain - nausea - vomiting - noticed a sudden change in bowel habits that last over 2 weeks
-
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. you need to use a stool softener laxative for more than 1 ...
-
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
Take only by mouth. Doses may be taken as a single daily dose or in divided doses. adults and children 12 years and overtake 1-3 capsules daily - children 2 to under 12 years of agetake 1 ...
-
Other information
each softgel contains: Sodium 5 mg - store at 25°C (77°F); excursion permitted between 15°-30°C (59°-86°F). Keep tightly closed.
-
Inactive ingredient
FD&C red no.40, FD&C yellow no.6, gelatin, glycerin, polyethylene glycol 400, propylene glycol, sorbitol sorbitan solution, water.
-
TAMPER EVIDENT
Do not use if safety seal under cap is broken or missing
-
Manufactured by
Softgel Healthcare Pvt. Ltd., Survey No. 20/1, Vandalur-Kelambakkam Road, Pudupakkam Village, Kancheepuram District, Tamilnadu - 603 103, India. Mfg. Lic. No.: XXXXXXXXXXXX
-
PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCEProduct Information