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 Doses may be taken as a single daily dose or in divided doses. Adults and children 12 years and over take 1-3 softgels daily Children 6 to under 12 years of age take 1 softgel daily Children under 6 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 Laxative
Ask a doctor before use if you
• have stomach pain, nausea or vomiting
• have a sudden change in bowel habits that persists over a period of 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.
| Adults and children 12 years and over | take 1-3 softgels daily |
| Children 6 to under 12 years of age | take 1 softgel daily |
| Children under 6 | 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.
FD&C red #40, FD&C yellow #6 (sunset yellow), gelatin, glycerin, PEG, sorbitol special, water.
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0307610414204 | GTIN-13: 0307610414204 EAN-13: 0307610414204 GTIN-12: 307610414204 UPC-A: 307610414204 GTIN storage (14 digits): 00307610414204 | 401BSDS.jpg |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 0761-0434 | 0761-0434-20 |
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 |
| MANNITOL | 3OWL53L36A | 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 |
|---|---|---|---|---|---|---|
| 4525bb51-0edc-eb63-e063-6394a90a485e | b8ce1cdd-2c22-1cbd-e053-2a95a90ae05d | 2025-12-04 | Warnings | 4525bb51-0edc-eb63-e063-6394a90a485e b8ce1cdd-2c22-1cbd-e053-2a95a90ae05d |
Adverse event summaries are temporarily unavailable. Other product information remains available.