Indications and uses
prevents / relieves dry hard stool results usually occur 1 to 3 days after the first dose
prevents / relieves dry hard stool results usually occur 1 to 3 days after the first dose
follow dosing directions below or take as directed by doctor must be given in a 6 to 8 oz glass of milk or fruit juice to prevent throat irritation may be taken as a single daily dose or in divided doses take maximum dose daily until first bowel movement, dosage should then be reduced according to individual response do not exceed recommended dose shake well before using Adults and children 12 years and over 1 to ...
Store at room temperature 15°-30°C (59°-86°F) protect from excessive heat Keep tightly closed Dispense in tight, light resistant container as defined in the USP for institutional use only each teaspoon (5 mL) contains: sodium 15 mg
Docusate Sodium 50 mg
Stool Softener
Do not use
Ask a doctor before use if you
Stop use and ask a doctor if
If pregnant or breast feeding, ask a health professional before use.
Keep out of reach of children. In case of accidental overdose, seek professional assisstance or contact a Poison Control Center immediately.
| Adults and children 12 years and over | 1 to 4 teaspoons (50 to 200 mg) |
| Children under 12 years of age | ask a doctor |
1 teaspoon = 5 mL
TAMPER EVIDENT: Do not use if breakaway band on cap is broken or missing.
citric acid, D&C Red #33, flavor, parabens, poloxamer, polyethylene glycol, sodium citrate, sorbitol, sucrose, and water.
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 57896-403-16 | ML - Milliliter | 57896-403 | f4cac32d-9b21-4812-9906-f5c952283548 | 1 | 2018-06-11 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 57896-403 | 57896-403-16 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ANHYDROUS CITRIC ACID | XF417D3PSL | IACT |
| D&C RED NO. 33 | 9DBA0SBB0L | IACT |
| METHYLPARABEN | A2I8C7HI9T | IACT |
| PROPYLPARABEN | Z8IX2SC1OH | IACT |
| POLYETHYLENE GLYCOL, UNSPECIFIED | 3WJQ0SDW1A | IACT |
| SODIUM CITRATE | 1Q73Q2JULR | IACT |
| WATER | 059QF0KO0R | IACT |
| POLOXAMER 407 | TUF2IVW3M2 | IACT |
| SUCROSE | C151H8M554 | IACT |
| SORBITOL | 506T60A25R | 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 |
|---|---|---|---|---|---|---|
| 9a008bb9-5625-fdd8-e053-2995a90a9d33 | 6bcb411a-f70f-058c-e053-2991aa0aa62a | 2019-12-18 | Warnings | 9a008bb9-5625-fdd8-e053-2995a90a9d33 6bcb411a-f70f-058c-e053-2991aa0aa62a |
Adverse event summaries are temporarily unavailable. Other product information remains available.