Stool Softener
- Product NDC
- 41163-778
- 11-digit product format
- 411630778
- Labeler code
- 41163
- Product ID
- 41163-778_b0672540-0f64-4d5d-ade2-16a05d40ba75
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- docusate sodium and sennosides
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- United Natural Foods, Inc. dba UNFI
- Application
- M007
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-06-25
- Substance
- DOCUSATE SODIUM; SENNOSIDES
- Active strength
- 50; 8.6 mg/1; 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
- Plus Stimulant
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DOCUSATE SODIUM | 50 mg/1 |
| SENNOSIDES | 8.6 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F05Q2T2JA0, 3FYP5M0IJX |
| Rxcui | 998740 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 41163-778-10 | Stool SoftenerPlus Stimulant | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41163-778 | STOOL SOFTENER PLUS STIMULANT (DOCUSATE SODIUM AND SENNOSIDES) TABLET [UNITED NATURAL FOODS, INC. DBA UNFI] | 3 | Current NDC, Legacy NDC, 1 package rows | 20240616_6c8c7c46-3ded-4e89-8e16-30eeb72aa08b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41163-778-10 | 41163077810 | 100 TABLET in 1 BOTTLE, PLASTIC (41163-778-10) | 100 tablet | 2021-06-25 | 0000-00-00 | No | No | Current |