Home NDC 72090-031-60 Senna Natural Relief
Product NDC 72090-031
Requested package NDC 72090-031-60
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 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 · 3 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 2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 72090-031 72090-031-60 I Inactivated by FDA excluded / ndc_excluded.zip fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 72090-031 72090-031-60 I Inactivated by FDA excluded / ndc_excluded.zip 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 72090-031 72090-031-60 I Inactivated by FDA excluded / ndc_excluded.zip 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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength 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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 72090-031-60 72090003160 600 TABLET in 1 BOTTLE (72090-031-60) 600 tablet 2020-08-03 0000-00-00 No No Current