Senna Plus

Product NDC: 71335-1181
Requested package NDC: 71335-1181-2
11-digit product format: 713351181
Labeler code: 71335
Product ID: 71335-1181_5f3b3624-f7a7-4cdf-8c23-d1bdea9b8038
Type: HUMAN OTC DRUG
Nonproprietary name: Sennosides and Docusate Sodium
Dosage form: TABLET
Route: ORAL
Labeler: Bryant Ranch Prepack
Application: part334
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2000-01-01
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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	71335-1181	71335-1181-2	D	Discontinued by firm		2026-10-05

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 · 14 matching rows.

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

Captured / source date, Code, Status table
Captured / source date	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-04-01 02:39 UTC · source 2025-03-31	I	Inactivated by FDA	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	I	Inactivated by FDA	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	I	Inactivated by FDA	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	I	Inactivated by FDA	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	I	Inactivated by FDA	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	I	Inactivated by FDA	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	I	Inactivated by FDA	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	I	Inactivated by FDA	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	I	Inactivated by FDA	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	I	Inactivated by FDA	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	I	Inactivated by FDA	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	I	Inactivated by FDA	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	I	Inactivated by FDA	`1332a3947898…`	`d4bfe170f9cd…`

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
NDC	Effective	Related label
71335-1181-1	2025-04-29	gc 455t (458)
71335-1181-2	2025-04-29	gc 455t (458)
71335-1181-3	2025-04-29	gc 455t (458)
71335-1181-4	2025-04-29	gc 455t (458)
71335-1181-5	2025-04-29	gc 455t (458)
71335-1181-6	2025-04-29	gc 455t (458)
71335-1181-7	2025-04-29	gc 455t (458)
71335-1181-8	2025-04-29	gc 455t (458)
71335-1181-9	2025-04-29	gc 455t (458)
71335-1181-1	2024-01-30	gc 455t (458)
71335-1181-2	2024-01-30	gc 455t (458)
71335-1181-3	2024-01-30	gc 455t (458)
71335-1181-4	2024-01-30	gc 455t (458)
71335-1181-5	2024-01-30	gc 455t (458)
71335-1181-6	2024-01-30	gc 455t (458)
71335-1181-7	2024-01-30	gc 455t (458)
71335-1181-8	2024-01-30	gc 455t (458)
71335-1181-9	2024-01-30	gc 455t (458)

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
71335-1181-2	EA - Each	71335-1181	60f5ef7c-0c36-4f9d-82b8-7a542a63f152	1	2021-02-05
71335-1181-3	EA - Each	71335-1181	108c2993-63f8-45a9-b2ba-691426cdf05d	1	2021-02-05
71335-1181-5	EA - Each	71335-1181	602eeab6-de3e-4f66-8672-0558ac24d431	1	2021-02-05
71335-1181-6	EA - Each	71335-1181	043bface-f714-4a2f-93d3-6b202403ada1	1	2021-02-05

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71335-1181	SENNA PLUS (SENNOSIDES AND DOCUSATE SODIUM) TABLET [BRYANT RANCH PREPACK]	3	Legacy NDC	20250430_5f3b3624-f7a7-4cdf-8c23-d1bdea9b8038.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
F05Q2T2JA0	DOCUSATE SODIUM	577-11-7	DOCUSATE SODIUM
3FYP5M0IJX	SENNOSIDES		SENNOSIDES

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
71335-1181-2	71335118102	120 TABLET in 1 BOTTLE (71335-1181-2)	120 tablet	2020-02-05	0000-00-00	No	No	Current