Senna

Product NDC: 71406-105
Requested package NDC: 71406-105-10
11-digit product format: 714060105
Labeler code: 71406
Product ID: 71406-105_ebe1e1fd-ec42-e0f0-e053-2995a90a2467
Type: HUMAN OTC DRUG
Nonproprietary name: Sennosides 8.6 mg Tablets
Dosage form: TABLET
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: SENNOSIDES
Active strength: 9 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	71406-105	71406-105-10	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 · 2 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	71406-105	71406-105-10	D	Discontinued by firm		excluded / ndc_excluded.zip	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	71406-105	71406-105-10	D	Discontinued by firm		excluded / ndc_excluded.zip	`f5e01cc5f278…`	`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
NDC	Effective	Related label
71406-105-01	2021-10-28	91320afc-2eec-692f-e053-2a95a90a3616
71406-105-10	2021-10-28	91320afc-2eec-692f-e053-2a95a90a3616
71406-105-01	2021-01-29	91320afc-2eec-692f-e053-2a95a90a3616
71406-105-10	2021-01-29	91320afc-2eec-692f-e053-2a95a90a3616

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
71406-105-01	EA - Each	71406-105	1c4ca8dd-59d6-498a-a0fb-024932d4ae22	1	2021-11-09
71406-105-10	EA - Each	71406-105	53afb42b-8473-41e5-9bea-2a02df8f9ae4	1	2021-11-09

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
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
71406-105-10	71406010510	1000 TABLET in 1 BOTTLE, PLASTIC (71406-105-10)	1000 tablet	2019-08-30	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Sennosides 8.6 mg Tablets - AACE PHARMACEUTICALS, INC.	AACE PHARMACEUTICALS, INC.	2024-11-07	HUMAN OTC DRUG LABEL	7
® Tablets	Bryant Ranch Prepack	2024-04-04	HUMAN OTC DRUG LABEL	103
® Tablets	Bryant Ranch Prepack	2024-04-04	HUMAN OTC DRUG LABEL	103