Indications and uses
for prevention of dry, hard stools for relief of occasional constipation this product usually produces a bowel movement in 12 to 72 hours
for prevention of dry, hard stools for relief of occasional constipation this product usually produces a bowel movement in 12 to 72 hours
do not give more than 45 mL in any 24 hour period use only with enclosed dosing cup find right dose on chart below mL = milliliter Age Dose Children 2 to under 12 years 15 mL to 45 mL; do not take more than 45 mL in 24 hours Children under 2 years ask a doctor Doses can be diluted in a suitable beverage to prevent throat irritation and to help mask the naturally tart flavor of the active ingredient (see side ...
Drug Facts
(in each 15 mL)
Docusate Sodium 50 mg
Stool softener
Drug Interaction Precaution: Do not give this product to your child if your child is presently taking mineral oil, unless directed by a doctor.
If constipation continues after 1 week of use, contact your child's doctor
These symptoms may be signs of a serious condition.
In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
| Age | Dose |
| Children 2 to under 12 years | 15 mL to 45 mL; do not take more than 45 mL in 24 hours |
| Children under 2 years | ask a doctor |
Doses can be diluted in a suitable beverage to prevent throat irritation and to help mask the naturally tart flavor of the active ingredient (see side panel for info).
citric acid, edetate disodium, flavor, methylparaben, polyethylene glycol, povidone, propylene glycol, propylparaben, sodium citrate, sorbitol, sucralose, water, xanthan gum, xylitol
1-866-255-6960 or
www.pedia-lax.com
Pedia-Lax
Docusate sodium
Liquid Stool Softener
4 fl oz (118 mL)
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 0132-0107 | 0132-0107-24 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| DOCUSATE SODIUM | F05Q2T2JA0 | ACTIB |
| CITRIC ACID MONOHYDRATE | 2968PHW8QP | IACT |
| EDETATE DISODIUM | 7FLD91C86K | IACT |
| METHYLPARABEN | A2I8C7HI9T | IACT |
| POLYETHYLENE GLYCOL, UNSPECIFIED | 3WJQ0SDW1A | IACT |
| POVIDONE | FZ989GH94E | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| PROPYLPARABEN | Z8IX2SC1OH | IACT |
| SODIUM CITRATE | 1Q73Q2JULR | IACT |
| SORBITOL | 506T60A25R | IACT |
| SUCRALOSE | 96K6UQ3ZD4 | IACT |
| WATER | 059QF0KO0R | IACT |
| XANTHAN GUM | TTV12P4NEE | IACT |
| XYLITOL | VCQ006KQ1E | 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 |
|---|---|---|---|---|---|---|
| 9850a9df-2dd8-45b5-b2d5-ed55901f9986 | 41f10fa8-2dd2-4fc5-ad29-b4f7a63ab3cb | 2024-10-17 | Warnings | 41f10fa8-2dd2-4fc5-ad29-b4f7a63ab3cb |
Adverse event summaries are temporarily unavailable. Other product information remains available.