Drug Facts:

Active Ingredient:
(in each softgel) Purpose:

Docusate sodium USP,
100 mg Stool Softener

Uses:

Temporary relief of occasional constipation.
This product generally produces bowel movement within 12 to 72 hours.

Warnings:

Do not use:

If abdominal pain, nausea or vomiting are present.

Ask a doctor before use if:

You have noticed a sudden change in bowel habits that persists over a period of 2 weeks.
You are presently taking mineral oil.

Stop use and ask a doctor if:

Rectal bleeding or failure to have a bowel movement occur after use, which may indicate a serious condition.
You need to use a laxative for more than 1 week.

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 immediately.

Directions:


Adults and children 12 years and over.	Take 1 to 3 softgels daily.
Children 2 to under 12 years.	Take 1 softgel daily.
Children under 2 years.	Ask a doctor.

Other Information

Each softgel contains: sodium, 5 mg
Store at 15-30°C (59-86°F).
Protect from excessive moisture.

Inactive Ingredients: FD&C Red #40, FD&C Yellow #6, gelatin, glycerin, polyethylene glycol, propylene glycol, purified water and sorbitol special.

How Supplied: Blister Pack of 10, and bottles of 25, 50, or 100 liquid gels.

Boehringer Ingelheim Consumer Healthcare Products.

Division of Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877

Questions about DULCOLAX?

Call toll-free 1-888-285-9159

*Among Stool Softener ingredients

PRODUCT PHOTO(S):

NOTE: These photos can be used only for identification by shape, color, and imprint. They do not depict actual or relative size.

The product samples shown here have been supplied by the manufacturer and reproduced in full color by PDR as a quick-reference identification aid. While every effort has been made to assure accurate reproduction, please remember that any visual identification should be considered preliminary. In cases of poisoning or suspected overdosage, the drug's identity should be verified by chemical analysis.