Stool Softener
- Product NDC
- 59726-058
- 11-digit product format
- 597260058
- Labeler code
- 59726
- Product ID
- 59726-058_eb9d2c44-06dd-4804-a2ee-40d39584bc9b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Docusate Sodium
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- M007
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-06-25
- Marketing end
- 2026-12-31
- Substance
- DOCUSATE SODIUM
- Active strength
- 250 mg/1
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Stool Softener
- Brand name suffix
- Extra Strength
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DOCUSATE SODIUM | 250 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F05Q2T2JA0 |
| Rxcui | 1245468 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59726-058-25 | Stool SoftenerExtra Strength | 250 in 1 BOTTLE | CAPSULE, LIQUID FILLED | 250 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59726-058 | STOOL SOFTENER EXTRA STRENGTH (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [P & L DEVELOPMENT, LLC] | 3 | Current NDC, Legacy NDC, 1 package rows | 20240501_4e97dd60-96e3-4b51-b614-c62480af1919.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59726-058-25 | 59726005825 | 250 CAPSULE, LIQUID FILLED in 1 BOTTLE (59726-058-25) | 2021-06-25 | 2026-12-31 | No | No | Current |