take with a glass of water adults and children 12 years of age and over 1 to 3 capsules daily. This dose may be taken as a single daily dose or in divided doses. children 2 to under 12 years of age 1 capsule daily children under 2 years of age ask a doctor
www.Dulcolax.comDulcolax® Stool Softener
Drug Facts
Docusate sodium (USP) 100 mg
Stool softener laxative
● for relief of occasional constipation and irregularity
● this product generally produces bowel movement in 12 to 72 hours
● if you are presently taking mineral oil, unless told to do so by a doctor
● stomach pain, nausea or vomiting
● a sudden change in bowel habits that lasts more than 2 weeks
● you have rectal bleeding or no bowel movement after using this product. These could be signs of a serious condition.
● you need to use a laxative for more than 1 week
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away.
take with a glass of water
adults and children 12 years of age and over 1 to 3 capsules daily. This dose may be taken as a single daily dose or in divided doses.
children 2 to under 12 years of age 1 capsule daily
children under 2 years of age ask a doctor
● each capsule contains: sodium 6 mg
● store at 20°-25°C (68°-77°F)
● protect from excessive humidity
● do not use this product if the safety seal under the cap is torn or missing
FD&C red no. 40, FD&C yellow no. 6, gelatin, glycerin, mannitol, pharmaceutical ink, polyethylene glycol 400, propylene glycol, sorbitan, sorbitol, water
Call 1-
866-844-2798 or visit www.Dulcolax.com
Dulcolax
Docusate sodium (USP) 100 mg/ Stool Softener Laxative
STOOL SOFTENER
STIMULANT-FREE
50
LIQUID GELS
Sugar Free
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 41167-0220-2 | EA - Each | 41167-0220 | bc7e279a-9959-4b39-90e2-0b510a71e62e | 1 | 2022-06-06 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 41167-0220 | 41167-0220-5, 41167-0220-4, 41167-0220-2, 41167-0220-3, 41167-0220-9, 41167-0220-6 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| DOCUSATE SODIUM | F05Q2T2JA0 | ACTIB |
| FD&C RED NO. 40 | WZB9127XOA | IACT |
| FD&C YELLOW NO. 6 | H77VEI93A8 | IACT |
| GELATIN | 2G86QN327L | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| MANNITOL | 3OWL53L36A | IACT |
| POLYETHYLENE GLYCOL 400 | B697894SGQ | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| SORBITAN | 6O92ICV9RU | IACT |
| SORBITOL | 506T60A25R | IACT |
| WATER | 059QF0KO0R | IACT |
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 59520d68-6e11-4cd5-80d6-1e4fdbfacf7b | 5c382fcc-a5e8-40f9-b5ae-5ed7a060b898 | 2021-03-08 | Warnings | 5c382fcc-a5e8-40f9-b5ae-5ed7a060b898 |
Adverse event summaries are temporarily unavailable. Other product information remains available.