Stool Softener Plus Stimulant Laxative
- Product NDC
- 49035-828
- 11-digit product format
- 490350828
- Labeler code
- 49035
- Product ID
- 49035-828_91614989-a4b0-4286-acd1-44748e89db1c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Docusate sodium, Sennosides
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- EQUATE (Wal-Mart Stores, Inc.)
- Application
- part334
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2019-02-28
- Marketing end
- 0000-00-00
- Substance
- DOCUSATE SODIUM; SENNOSIDES
- Active strength
- 50 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 49035-828 | D | Discontinued by firm | 2026-08-03 | ||
| excluded package | package | 49035-828 | 49035-828-12 | D | Discontinued by firm | 2026-08-03 | |
| excluded package | package | 49035-828 | 49035-828-24 | D | Discontinued by firm | 2026-08-03 |
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Package NDC | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded product | product | d630ba8d3edf… | 732f749b63fb… | |
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 49035-828-12 | d630ba8d3edf… | 732f749b63fb… |
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 49035-828-24 | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded product | product | f5e01cc5f278… | a2eaf40c39c3… | |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 49035-828-12 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 49035-828-24 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | excluded product | product | 2ef7874e63bc… | 57b86245f4fa… | |
| 2025-04-01 02:39 UTC · source 2025-03-31 | excluded package | package | 49035-828-12 | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | excluded package | package | 49035-828-24 | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | excluded product | product | a1b67e2a42f9… | c4cf2c586c0d… | |
| 2025-03-28 20:22 UTC · source 2025-03-28 | excluded package | package | 49035-828-12 | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | excluded package | package | 49035-828-24 | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded product | product | cfe11265f3b6… | 090c488252e2… | |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded package | package | 49035-828-12 | cfe11265f3b6… | 090c488252e2… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | excluded package | package | 49035-828-24 | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded product | product | cdf11ea48f46… | ba0047e9e063… | |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded package | package | 49035-828-12 | cdf11ea48f46… | ba0047e9e063… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | excluded package | package | 49035-828-24 | cdf11ea48f46… | ba0047e9e063… |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Related label |
|---|---|---|
| 49035-828-12 | 2020-11-03 | DRUG FACTS |
| 49035-828-24 | 2020-11-03 | DRUG FACTS |
| 49035-828-12 | 2020-09-27 | DRUG FACTS |
| 49035-828-24 | 2020-09-27 | DRUG FACTS |
| 49035-828-12 | 2020-09-25 | DRUG FACTS |
| 49035-828-24 | 2020-09-25 | DRUG FACTS |
| 49035-828-12 | 2020-07-22 | DRUG FACTS |
| 49035-828-24 | 2020-07-22 | DRUG FACTS |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 49035-828-12 | EA - Each | 49035-828 | 67c4426f-562e-411c-98df-fd3d5b23fc86 | 1 | 2024-05-16 |
| 49035-828-24 | EA - Each | 49035-828 | c4d54623-fff3-4f9c-a2e3-85c09d89446e | 1 | 2019-11-12 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 49035-828-12 | 49035082812 | 120 TABLET in 1 BOTTLE, PLASTIC (49035-828-12) | 120 tablet | 2019-02-28 | 0000-00-00 | No | No | Current |
| 49035-828-24 | 49035082824 | 240 TABLET in 1 BOTTLE, PLASTIC (49035-828-24) | 240 tablet | 2019-02-28 | 0000-00-00 | No | No | Current |