FDA.reportPublic FDA data

Stool Softener Plus Stimulant Laxative

Product NDC
49035-828
Requested package NDC
49035-828-24
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.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage49035-82849035-828-24DDiscontinued by firm2026-08-03

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.

Historic NDC status page 1 of 1 · 6 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
49035-828-122020-11-03DRUG FACTS
49035-828-242020-11-03DRUG FACTS
49035-828-122020-09-27DRUG FACTS
49035-828-242020-09-27DRUG FACTS
49035-828-122020-09-25DRUG FACTS
49035-828-242020-09-25DRUG FACTS
49035-828-122020-07-22DRUG FACTS
49035-828-242020-07-22DRUG FACTS

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49035-828-12EA - Each49035-82867c4426f-562e-411c-98df-fd3d5b23fc8612024-05-16
49035-828-24EA - Each49035-828c4d54623-fff3-4f9c-a2e3-85c09d89446e12019-11-12

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
49035-828-2449035082824240 TABLET in 1 BOTTLE, PLASTIC (49035-828-24) 240 tablet2019-02-280000-00-00NoNoCurrent