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 ...
Docusate Sodium 50 mg
Stool Softener
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 6 teaspoons (50 to 300 mg) |
| Children 2 to 12 years of age | 1 to 3 teaspoons (50 to 150 mg) |
1 teaspoon = 5 mL
TAMPER EVIDENT: Do not use if breakaway band on cap is broken or missing.
Other information
citric acid, D&C Red #33, flavor, methylparaben, parabens, poloxamer, polyethylene glycol 400, propylparaben, sodium citrate, sorbitol, sucrose, and water.
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 1248119 | docusate sodium 50 MG in 5 mL Oral Suspension | PSN | 1 |
| 1248119 | docusate sodium 10 MG/ML Oral Suspension | SCD | 1 |
| 1248119 | docusate sodium 100 MG per 10 ML Oral Suspension | SY | 1 |
| 1248119 | docusate sodium 150 MG per 15 ML Oral Suspension | SY | 1 |
| 1248119 | docusate sodium 50 MG per 5 ML Oral Suspension | SY | 1 |
| 1248119 | DOSS Sodium 10 MG/ML Oral Suspension | SY | 1 |
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| d5e51f11-ad28-caa4-4b49-4143974782ad | Product name | 1 | 20150831 |
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 54162-195-16 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-e401-f424-e053-dadaa90a57ce | Docusate Sodium Liquid |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 54162-195-16 | Docusate Sodium Liquid | 473 mL in 1 BOTTLE, PLASTIC | LIQUID | 473 | 1 |
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 54162-195-16 | ML - Milliliter | 54162-195 | 770e890c-0030-4f83-af1a-9754e4754291 | 1 | 2018-01-12 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 54162-195 | 54162-195-16 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Docusate sodium | F05Q2T2JA0 | ACTIB |
| anhydrous citric acid | XF417D3PSL | IACT |
| D&C red no. 33 | 9DBA0SBB0L | IACT |
| methylparaben | A2I8C7HI9T | IACT |
| propylparaben | Z8IX2SC1OH | IACT |
| POLYETHYLENE GLYCOL 400 | B697894SGQ | IACT |
| sodium citrate | 1Q73Q2JULR | IACT |
| water | 059QF0KO0R | IACT |
| Poloxamer 407 | TUF2IVW3M2 | IACT |
| SUCROSE | C151H8M554 | IACT |
| SORBITOL | 506T60A25R | IACT |
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 |
|---|---|---|---|---|---|---|
| 6b770ed5-fd3f-4797-a693-6724b73c7758 | 4d022ef5-fa76-4e50-b56b-759bc35754ab | 2017-09-28 | Warnings | 6b770ed5-fd3f-4797-a693-6724b73c7758 4d022ef5-fa76-4e50-b56b-759bc35754ab |
Adverse event summaries are temporarily unavailable. Other product information remains available.