Senna Natural Relief

Product NDC: 72090-031
Requested package NDC: 72090-031-10
11-digit product format: 720900031
Labeler code: 72090
Product ID: 72090-031_51f79e6b-89ca-4116-9ae9-1d6f191c1a66
Type: HUMAN OTC DRUG
Nonproprietary name: Senna Natural Relief
Dosage form: TABLET
Route: ORAL
Labeler: Pioneer Life Sciences, LLC
Application: 505G(a)(3)
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2024-10-03
Substance: SENNOSIDES
Active strength: 8.6 mg/1
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

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	72090-031	72090-031-10	I	Inactivated by FDA		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 · 18 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	`1332a3947898…`	`d4bfe170f9cd…`
2022-08-30 03:57 UTC · source 2022-08-29	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	`bd6a592717d7…`	`303034d00443…`

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: Senna Natural Relief
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
SENNOSIDES	8.6 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
3FYP5M0IJX	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
312935	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
ce0938d4-efd1-4efb-8e51-037f7040080e	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72090-031-60	2023-10-25	C162847	48780-1	d6a99b39-e015-a426-e053-dadaa90af4c2	ac8b602a-e53c-0b44-e053-2a95a90affa8
72090-031-10	2022-01-28	C162847	48780-1	d6a99b39-9323-a426-e053-dadaa90af4c2	ac8c3b11-8068-59e6-e053-2a95a90a3256
72090-031-60	2022-01-28	C162847	48780-1	d6a99b39-e015-a426-e053-dadaa90af4c2	ac8b602a-e53c-0b44-e053-2a95a90affa8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
72090-031-60	Senna Natural Relief	600 in 1 BOTTLE	TABLET	600	4
72090-031-02	Senna Natural Relief	300 in 1 BOTTLE	TABLET	300	2
72090-031-10	Senna Natural Relief	1000 in 1 BOTTLE	TABLET	1000	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72090-031	SENNA NATURAL RELIEF TABLET [PIONEER LIFE SCIENCES, LLC]	3	Current NDC, Legacy NDC, 1 package rows	20241127_ac8b602a-e53c-0b44-e053-2a95a90affa8.zip
72090-031	SENNA NATURAL RELIEF TABLET [PIONEER LIFE SCIENCES, LLC]	1	Current NDC, Legacy NDC, 1 package rows	20241006_ce0938d4-efd1-4efb-8e51-037f7040080e.zip
72090-031	SENNA NATURAL RELIEF TABLET [PIONEER LIFE SCIENCES, LLC]	1	Current NDC, Legacy NDC, 1 package rows	20200811_ac8c3b11-8068-59e6-e053-2a95a90a3256.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Senna Natural Relief	SENNA NATURAL RELIEF	Pioneer Life Sciences, LLC	ce0938d4-efd1-4efb-8e51-037f7040080e	2025-12-29	Warnings	Exact identifier ndc (product): 72090-031
Senna Natural Relief	SENNA NATURAL RELIEF	Pioneer Life Sciences, LLC	ac8b602a-e53c-0b44-e053-2a95a90affa8	2025-12-29	Warnings	Exact identifier ndc (product): 72090-031

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
3FYP5M0IJX	SENNOSIDES	SENNOSIDES

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
312935	sennosides 8.6 MG Oral Tablet	PSN	ac8b602a-e53c-0b44-e053-2a95a90affa8	4
312935	sennosides, USP 8.6 MG Oral Tablet	SCD	ac8b602a-e53c-0b44-e053-2a95a90affa8	4
312935	sennosides A and B 8.6 MG Oral Tablet	SY	ac8b602a-e53c-0b44-e053-2a95a90affa8	4
312935	sennosides 8.6 MG Oral Tablet	PSN	ce0938d4-efd1-4efb-8e51-037f7040080e	2
312935	sennosides, USP 8.6 MG Oral Tablet	SCD	ce0938d4-efd1-4efb-8e51-037f7040080e	2
312935	sennosides A and B 8.6 MG Oral Tablet	SY	ce0938d4-efd1-4efb-8e51-037f7040080e	2
312935	sennosides 8.6 MG Oral Tablet	PSN	ac8c3b11-8068-59e6-e053-2a95a90a3256	1
312935	sennosides, USP 8.6 MG Oral Tablet	SCD	ac8c3b11-8068-59e6-e053-2a95a90a3256	1
312935	sennosides A and B 8.6 MG Oral Tablet	SY	ac8c3b11-8068-59e6-e053-2a95a90a3256	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
72090-031-10	72090003110	1000 TABLET in 1 BOTTLE (72090-031-10)	1000 tablet	2020-08-03	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Senna Natural Relief - Pioneer Life Sciences, LLC	Pioneer Life Sciences, LLC	2025-12-29	HUMAN OTC DRUG LABEL	4
Senna Natural Relief - Pioneer Life Sciences, LLC	Pioneer Life Sciences, LLC	2025-12-29	HUMAN OTC DRUG LABEL	2
Senna Natural Relief - Pioneer Life Sciences, LLC	Pioneer Life Sciences, LLC	2020-08-10	HUMAN OTC DRUG LABEL	1