Stool Softener
- Product NDC
- 41250-859
- 11-digit product format
- 412500859
- Labeler code
- 41250
- Product ID
- 41250-859_58d88467-31db-4f6d-986c-bef786e585fb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Docusate Sodium
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- MEIJER, INC.
- Application
- M007
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-12-27
- Substance
- DOCUSATE SODIUM
- Active strength
- 250 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Stool Softener
- Brand name suffix
- Extra Strength
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DOCUSATE SODIUM | 250 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F05Q2T2JA0 |
| Rxcui | 1245468 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 41250-859-10 | Stool SoftenerExtra Strength | 100 in 1 BOTTLE, PLASTIC | CAPSULE, LIQUID FILLED | 100 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41250-859 | STOOL SOFTENER EXTRA STRENGTH (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [MEIJER, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20231013_e43bd2ed-17c7-4530-af72-81a7ad70069c.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 |
|---|
| 41250-859-10 | 41250085910 | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (41250-859-10) | 2019-12-27 | 0000-00-00 | No | No | Current |