Indications and uses
relieves occasional constipation (irregularity) generally produces bowel movement in 12 to 72 hours
relieves occasional constipation (irregularity) generally produces bowel movement in 12 to 72 hours
do not exceed recommended dose adults and children 12 years and older: take 1-3 softgels daily, until first bowel movement; 1 softgel daily thereafter, or as directed by a doctor children under 12: ask a doctor
• each softgel contains: sodium 7 mg. Very low sodium • store at 59°-77°F (15°-25°C) • keep tightly closed • Tamper Evident: Do not use if imprinted seal under cap is missing or broken.
Docusate Sodium 100 mg
Stool Softener
Ask a doctor before use if you
• have stomach pain, nausea or vomiting
• noticed a sudden change in bowel habits that lasts for over 2 weeks
• are presently taking mineral oil
Stop use and ask a doctor if
• you need to use a laxative longer than 1 week
• you have rectal bleeding or fail to have a bowel movement. These
could be signs of 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.
•
each softgel contains: sodium 7 mg. Very low sodium
• store at 59°-77°F (15°-25°C)
• keep tightly closed
•
Tamper Evident: Do not use if imprinted seal
under cap is missing or broken.
FD&C red #40, FD&C yellow #6 (sunset yellow), gelatin, glycerol, PEG, sorbitol special, purified water.
1-800-540-3765
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0385111401107 | GTIN-13: 0385111401107 EAN-13: 0385111401107 GTIN-12: 385111401107 UPC-A: 385111401107 GTIN storage (14 digits): 00385111401107 | 401-crw.jpg |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 85111-401-10 | Stool Softener | 1000 in 1 BOTTLE | CAPSULE, LIQUID FILLED | 1000 | 1 | |
| 85111-401-50 | Stool Softener | 500 in 1 BOTTLE | CAPSULE, LIQUID FILLED | 500 | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 85111-401 | 85111-401-10, 85111-401-50 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| FD&C RED NO. 40 | WZB9127XOA | IACT |
| GELATIN | 2G86QN327L | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| POLYETHYLENE GLYCOL 400 | B697894SGQ | IACT |
| SORBITOL | 506T60A25R | IACT |
| WATER | 059QF0KO0R | IACT |
| FD&C YELLOW NO. 6 | H77VEI93A8 | IACT |
| DOCUSATE SODIUM | F05Q2T2JA0 | ACTIB |
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 |
|---|---|---|---|---|---|---|
| Stool Softener | DOCUSATE SODIUM | RMT HEALTH LLC | 44fbb197-fe90-c5a8-e063-6394a90adb7d | 2025-12-02 | Warnings | 85111-401-50 85111-401-10 85111-401 85111040150 85111040110 44fbb054-2c67-2bdd-e063-6294a90ad938 44fbb197-fe90-c5a8-e063-6394a90adb7d |
Adverse event summaries are temporarily unavailable. Other product information remains available.