Stool Softener
- Product NDC
- 21130-878
- 11-digit product format
- 211300878
- Labeler code
- 21130
- Product ID
- 21130-878_047a9d14-a528-4ac5-8a25-ed236e4a3baa
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- docusate sodium and sennosides
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Safeway, Inc.
- Application
- M007
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-09-30
- 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 Laxative
- 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 |
|---|
| 21130-878-20 | Stool SoftenerPlus Stimulant Laxative | 200 in 1 BOTTLE, PLASTIC | TABLET | 200 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21130-878 | STOOL SOFTENER PLUS STIMULANT LAXATIVE (DOCUSATE SODIUM AND SENNOSIDES) TABLET [SAFEWAY, INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20240517_6bc9ea37-31b8-4a6d-9b2d-2c80bad4f30d.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 |
|---|
| 21130-878-20 | 21130087820 | 200 TABLET in 1 BOTTLE, PLASTIC (21130-878-20) | 200 tablet | 2020-09-30 | 0000-00-00 | No | No | Current |