FDA.reportPublic FDA data

Senna-S

Product NDC
71406-106
11-digit product format
714060106
Labeler code
71406
Product ID
71406-106_eb8f0eab-a05c-c489-e053-2995a90a4f17
Type
HUMAN OTC DRUG
Nonproprietary name
Docusate Sodium 50 mg Sennosides 8.6 mg
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
AACE PHARMACEUTICALS, INC.
Application
part334
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2019-08-30
Marketing end
0000-00-00
Substance
DOCUSATE SODIUM; SENNOSIDES
Active strength
50 mg/1; mg/1
NDC exclude flag
No
Listing certified through
2023-12-31
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 · 3 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct71406-106DDiscontinued by firm2026-10-05
excluded packagepackage71406-10671406-106-01DDiscontinued by firm2026-10-05
excluded packagepackage71406-10671406-106-10DDiscontinued by firm2026-10-05

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, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage71406-106-10d630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage71406-106-01d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage71406-106-10f5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage71406-106-01f5e01cc5f278…a2eaf40c39c3…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
71406-106-012021-10-2991426a5b-dc03-a27b-e053-2a95a90a8ff8
71406-106-062021-10-2991426a5b-dc03-a27b-e053-2a95a90a8ff8
71406-106-102021-10-2991426a5b-dc03-a27b-e053-2a95a90a8ff8
71406-106-012021-01-2991426a5b-dc03-a27b-e053-2a95a90a8ff8
71406-106-062021-01-2991426a5b-dc03-a27b-e053-2a95a90a8ff8
71406-106-102021-01-2991426a5b-dc03-a27b-e053-2a95a90a8ff8

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71406-106-01EA - Each71406-106f9c40606-8818-4f2b-860d-2c879d9100d512021-11-09
71406-106-10EA - Each71406-10648c2bece-df8f-4c88-ad77-57a69f41f09d12021-11-09

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71406-106-0171406010601100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71406-106-01) 2019-08-300000-00-00NoNoCurrent
71406-106-10714060106101000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71406-106-10) 2019-08-300000-00-00NoNoCurrent