OTC - ACTIVE INGREDIENT SECTION
Docusate Sodium 50 mg
Sennosides 8.6 mg
Docusate Sodium 50 mg
Sennosides 8.6 mg
relieves occasional constipation (irregularity)
generally produces bowel movement in 6 to 12 hours
Docusate Sodium 50 mg
Sennosides 8.6 mg
Do not use for more than 1 week unless directed by a doctor
Ask a doctor before use if you -have abdominal pain, nausea or vomiting -are taking mineral oil -have noticed a sudden change in bowel habits that lasts over 2 weeks
Stop use and ask a doctor if -you have no bowel movement within 12 hours -you have rectal bleeding. these could 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.
do not exceed 8 tablets in 24 hours
Age
Starting Dose
Maximum Dose
adults and children 12 years of age and older
2 tablets once a day preferably at bedtime; increase as needed, or as directed by a doctor
4 tablets in the morning and 4 tablets at bedtime
children under 12 years
ask a doctor
each tablet contains: calcium 7 mg
• store at room temperature
cellulose, croscarmellose sodium, dicalcium phosphate, FD and C yellow no. 5 (tartrazine), FD and C yellow no. 6, hypromellose, magnesium silicate, magnesium stearate, mineral oil, PEG, sodium benzoate, sodium lauryl sulfate, starch, stearic acid, titanium dioxide, triacetin
o not exceed 8 tablets in 24 hours
Age
Starting Dose
Maximum Dose
adults and children 12 years of age and older
2 tablets once a day preferably at bedtime; increase as needed, or as directed by a doctor
4 tablets in the morning and 4 tablets at bedtime
children under 12 years
ask a doctor
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 57896-455-01 | EA - Each | 57896-455 | 0f219bae-0f6b-42bf-b51b-1eabc0b9b748 | 1 | 2013-05-02 |
| 57896-455-06 | EA - Each | 57896-455 | 998bed0f-dc2d-4ae5-8192-7e025d26cbc8 | 1 | 2015-07-20 |
| 57896-455-10 | EA - Each | 57896-455 | 9eb9f425-a2c3-4683-bc38-aa178b0407f3 | 1 | 2018-04-19 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 61919-684 | 61919-684-60 |
| 57896-455 |
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| 071193ac-34dc-244b-e063-6294a90a9e7c | 830d195a-d5d5-b3e5-e053-2991aa0aee2a | 2023-10-06 | Warnings | 830d195a-d5d5-b3e5-e053-2991aa0aee2a |
Adverse event summaries are temporarily unavailable. Other product information remains available.