Sennosides

Product NDC
37808-712
11-digit product format
378080712
Labeler code
37808
Product ID
37808-712_46537594-decb-ce80-e063-6394a90aa159
Type
HUMAN OTC DRUG
Nonproprietary name
Sennosides
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
H E B
Application
M007
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-07-31
Substance
SENNOSIDES
Active strength
17.2 mg/17.21
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 · 10 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCCodeStatusSnapshotSource SHA-256
2025-03-22 03:12 UTC · source 2025-03-21excluded productproductIInactivated by FDAcfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-21excluded packagepackage37808-712-10IInactivated by FDAcfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10excluded productproductIInactivated by FDAcdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-10excluded packagepackage37808-712-10IInactivated by FDAcdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31excluded productproductUExcluded because listing certification expired302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-31excluded packagepackage37808-712-10UExcluded because listing certification expired302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20excluded productproductUExcluded because listing certification expireded331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-20excluded packagepackage37808-712-10UExcluded because listing certification expireded331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10excluded productproductUExcluded because listing certification expired0efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage37808-712-10UExcluded because listing certification expired0efc9e666f02…f202fb6c5f17…

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
Sennosides
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SENNOSIDES17.2 mg/17.21

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3FYP5M0IJXInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
2169295Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
a5652d5b-43fd-5bfa-e053-2995a90aad6cAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
baf7f49c-75b6-496b-a00e-8e766a8e4f03Product name120210127
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37808-712-10Sennosides100 in 1 BOTTLECAPSULE, LIQUID FILLED1007

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37808-712SENNOSIDES CAPSULE, LIQUID FILLED [H E B]5Current NDC, Legacy NDC, 1 package rows20250322_a5652d5b-43fd-5bfa-e053-2995a90aad6c.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 30 of 42 · 833 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Senna-LaxSENNOSIDESGuardian Drug Companyd3ee7288-986e-44a6-8aa2-05405210c8752024-12-19WarningsExact identifier
application number: M007
Quality Choice Stool SoftenerDOCUSATE SODIUMChain Drug Marketing Association4d5facd4-f57f-44f7-b8dd-83a33e57afd92024-12-18WarningsExact identifier
application number: M007
Good Neighbor Pharmacy Gentle LaxativeBISACODYLAmerisourceBergen Drug Corp8336d821-ec70-468e-98b2-512a9a7212e02024-12-18WarningsExact identifier
application number: M007
Good Neighbor Stool SoftenerDOCUSATE SODIUMAmerisourceBergen Drug Corp88d657a1-77be-412a-9295-034872db2dde2024-12-18WarningsExact identifier
application number: M007
Preferred Stool SoftenerDOCUSATE SODIUMReese Pharmaceutical Co217d13a0-3205-492c-af49-82eb80dba53a2024-12-18WarningsExact identifier
application number: M007
Preferred Stool SoftenerDOCUSATE CALCIUMReese Pharmaceutical Co3b481b74-5683-466f-ad74-3da63279ce912024-12-18WarningsExact identifier
application number: M007
Topcare Stool SoftenerDOCUSATE SODIUMTOPCO ASSOCIATES LLC9342c1b5-5d35-4b60-b347-c208c0774cdc2024-12-18WarningsExact identifier
application number: M007
HEB Stool SoftenerDOCUSATE SODIUMH E B3a513cb9-8404-43dc-a780-040bf9f1741d2024-12-18WarningsExact identifier
application number: M007
Topcare Stool Softener laxativeDOCUSATE SODIUMTOPCO ASSOCIATES LLCf9302fc2-684d-4cc2-bdd7-7ad0e9304edb2024-12-18WarningsExact identifier
application number: M007
Good Neighbor Stool Softener laxativeDOCUSATE SODIUMAmerisourceBergen Drug Corpd09151ae-1cc6-4e69-8d80-7813082a42362024-12-18WarningsExact identifier
application number: M007
Dollar General Gentle LaxativeBISACODYLDolgencorp, LLCf1977a2e-942a-49eb-8d0f-cdb67b020a262024-12-18WarningsExact identifier
application number: M007
Discount Drugmart Gentle LaxativeBISACODYLDiscount Drug Mart, Incb525a0a9-f97c-4406-8360-58e87e44cfce2024-12-18WarningsExact identifier
application number: M007
HEB Gentle LaxativeBISACODYLH E B3d163d71-93c7-419f-9707-5811aa6474fb2024-12-18WarningsExact identifier
application number: M007
Winco Stool SoftenerDOCUSATE SODIUMWinCo Foods, LLC4de2e315-5ec6-4ddf-8617-4e07ba4563542024-12-18WarningsExact identifier
application number: M007
Meijer Gentle LaxativeBISACODYLMeijer Distribution Inc.b49786a1-f0b9-45ae-b8f6-683489c54e762024-12-18WarningsExact identifier
application number: M007
H E B Stool Softener laxativeDOCUSATE SODIUMH E B9d848fdd-3a2f-45c6-9ff3-17f1d74e0f4f2024-12-18WarningsExact identifier
application number: M007
Preferred Stool Softener laxativeDOCUSATE SODIUMReese Pharmaceutical Co9135addd-4fc7-411b-b3c3-79e7e0e4cec82024-12-18WarningsExact identifier
application number: M007
DOCUSATE SODIUM 100mg Two-ToneDOCUSATE SODIUMDiscount Drug Mart, Inc80092188-0517-4646-bd46-ab56c63bb3542024-12-18WarningsExact identifier
application number: M007
Winco Stool SoftenerDOCUSATE SODIUMWinCo Foods, LLCd74c54d6-7a75-4ca9-8425-7593b7841b0f2024-12-18WarningsExact identifier
application number: M007
Quality Choice Stool Softener laxativeDOCUSATE SODIUMChain Drug Marketing Association7635b081-4350-45d0-b44e-82afccce21342024-12-18WarningsExact identifier
application number: M007

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2169295sennosides 17.2 MG Oral CapsulePSNa5652d5b-43fd-5bfa-e053-2995a90aad6c7
2169295sennosides, USP 17.2 MG Oral CapsuleSCDa5652d5b-43fd-5bfa-e053-2995a90aad6c7
2169295sennosides 17.2 MG Oral CapsuleSYa5652d5b-43fd-5bfa-e053-2995a90aad6c7

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
37808-712-1037808071210100 CAPSULE, LIQUID FILLED in 1 BOTTLE (37808-712-10) 2020-07-310000-00-00NoNoCurrent