Indications and uses
for overnight relief from occasional constipation (irregularity) generally produces bowel movement in 6 to12 hours
Stool Softener with Stimulant Laxative
- Manufacturer
- P & L Development, LLC
- Effective date
- 2021-10-26
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:30:31
Label at a glance#
ProductStool Softener with Stimulant Laxative
Active ingredientDOCUSATE SODIUM, SENNOSIDES
Label structure10 sections
Dosage and administration
Take only by mouth. Doses may be taken as a single daily dose, preferably in the evening, or in divided doses. adults and children 12 years and older take 2-4 tablets daily children 6 to under 12 years of age take 1-2 tablets daily children 2 to under 6 years of age take up to 1 tablet daily children under 2 ask a doctor
Contacts and useful links#
Label contents#
Full prescribing information#
Active ingredients (in each tablet)
Docusate sodium 50 mg
Sennosides 8.6 mg
Purpose
Stool softener
Stimulant laxative
Uses
- for overnight relief from occasional constipation (irregularity)
- generally produces bowel movement in 6 to12 hours
Warnings
Do not use
- laxative products for longer than 1 week unless directed by a doctor
- if you are now 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 lasts over a period of 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 may indicate 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
- Take only by mouth. Doses may be taken as a single daily dose, preferably in the evening, or in divided doses.
| adults and children 12 years and older | take 2-4 tablets daily |
| children 6 to under 12 years of age | take 1-2 tablets daily |
| children 2 to under 6 years of age | take up to 1 tablet daily |
| children under 2 | ask a doctor |
Other information
- each tablet contains: calcium 20 mg
- each tablet contains: sodium 6 mg VERY LOW SODIUM
- store at 25ºC (77ºF); excursions permitted between 15-30ºC(59-86ºF)
Inactive ingredients
carnauba wax*, croscarmellose sodium, dibasic calcium phosphate dihydrate, FD&C blue #2 aluminum lake, FD&C red #40 aluminum lake, hypromellose, magnesium stearate, maltodextrin*, microcrystalline cellulose, polyethylene glycol*, polyvinyl alcohol*, silcon dioxide, sodium benzoate*, stearic acid, talc*, titanium dioxide
*contains one or more of these ingredients
Questions or comments?
Call 1-877-753-3935 Monday-Friday 9AM-5PM EST
Principal Display Panel
stool softener + stimulant laxative
docusate sodium 50 mg
(stool softener )
sennosides 8.6 mg
(stimulant laxative)
tablets
†Compare to the active ingredients in Peri-Colace®
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.
**This product is not manufactured or distributed by Purdue Products LP., distributor of Peri-Colace®.
Distributed by: PL Developments
200 Hicks Street, Westbury, NY 11590
Product Label
Products#
Every source-derived product name is available through these pages.
- Stool Softener with Stimulant Laxative
- docusate sodium and sennosides
- DOCUSATE SODIUM
- DOCUSATE
- SENNOSIDES
- CARNAUBA WAX
- CROSCARMELLOSE SODIUM
- DIBASIC CALCIUM PHOSPHATE DIHYDRATE
- FD&C RED NO. 40
- HYPROMELLOSES
- MAGNESIUM STEARATE
- MALTODEXTRIN
- CELLULOSE, MICROCRYSTALLINE
- POLYETHYLENE GLYCOL, UNSPECIFIED
- SILICON DIOXIDE
- SODIUM BENZOATE
- STEARIC ACID
- TALC
- TITANIUM DIOXIDE
- ALUMINUM OXIDE
- FD&C BLUE NO. 2
- POLYVINYL ALCOHOL, UNSPECIFIED
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 59726-084 | 59726-084-10, 59726-084-40 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
openFDA label cross-check#
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 |
|---|---|---|---|---|---|---|
| 661486da-69ac-4f33-b507-d22b6f62a6e1 | b18b53e6-1f14-4942-95d6-e91cae4ed4de | 2021-10-26 | Warnings | 661486da-69ac-4f33-b507-d22b6f62a6e1 b18b53e6-1f14-4942-95d6-e91cae4ed4de |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.