FDA.reportPublic FDA data

Sennosides

Product NDC
0904-7252
11-digit product format
009047252
Labeler code
0904
Product ID
0904-7252_289eb036-6a1f-4d89-e063-6394a90ac159
Type
HUMAN OTC DRUG
Nonproprietary name
Sennosides
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Major Pharmaceuticals
Application
M007
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2022-05-17
Substance
SENNOSIDES
Active strength
8.6 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

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
SENNOSIDES8.6 mg/1

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
312935Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
df3b431b-a1ad-91dd-e053-2995a90aa02fAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0904-7252-60Sennosides100 in 1 BOTTLETABLET, FILM COATED1002
0904-7252-61Sennosides10 in 1 BLISTER PACKTABLET, FILM COATED102
0904-7252-61Sennosides10 in 1 BOX, UNIT-DOSETABLET, FILM COATED102
0904-7252-80Sennosides1000 in 1 BOTTLETABLET, FILM COATED10002

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0904-7252-60EA - Each0904-72528b411302-6cf8-4c67-887c-46174dec28f112023-03-13
0904-7252-61EA - Each0904-72524c7910a9-1558-4a7a-b204-d7064779beea12023-04-07
0904-7252-80EA - Each0904-725270b43092-f10c-4350-9488-9b7bae9b8d2512023-03-13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0904-7252SENNOSIDES TABLET, FILM COATED [MAJOR PHARMACEUTICALS]2Current NDC, Legacy NDC, 4 package rows20241208_df3b431b-a1ad-91dd-e053-2995a90aa02f.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 8 of 42 · 833 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LaxomilBISACODYL 5MGPharmadel LLC3999935b-d8e8-52a6-e063-6294a90aa2a22026-03-20WarningsExact identifier
application number: M007
Laxative Enteric CoatedBISACODYL 5MGGrocery Outletc820e6a1-fa23-447a-9ee9-50a1bd617adb2026-03-19WarningsExact identifier
application number: M007
CITRUCELMETHYLCELLULOSEHaleon US Holdings LLC9d5f2244-a610-4d45-b6e8-e79bb17a558f2026-03-18WarningsExact identifier
application number: M007
Stool Softener LaxativeDOCUSATE SODIUMSafeway, Inc.f178b31d-4843-4b91-a0d5-ab5ade835dc22026-03-16WarningsExact identifier
application number: M007
Stool Softener LaxativeDOCUSATE SODIUMSafeway, Inc.12ab9c3c-1f4b-43cd-83ac-b5f80b1aa54c2026-03-13WarningsExact identifier
application number: M007
Castor OilCASTOR OILOld East Main Co.a1ca668a-3bf9-46a9-8a4f-5cb61547bb812026-03-12Warnings, Adverse reactionsExact identifier
application number: M007
Castor OilCASTOR OILVi-Jon, LLCb29775df-8470-4fe3-bee3-f0490ea6903f2026-03-12WarningsExact identifier
application number: M007
Castor OilCASTOR OILNice-Pak Products, LLCcc43d514-ee82-4314-99b2-c64380f987792026-03-12Warnings, Adverse reactionsExact identifier
application number: M007
FiberconCALCIUM POLYCARBOPHILFoundation Consumer Brands7992a4bb-5535-4a1d-867d-a99f7e0c1be72026-03-12WarningsExact identifier
application number: M007
Stool Softener LaxativeDOCUSATE SODIUMWalgreenscda27a9c-9175-4b07-9c0b-d8d8978829652026-03-12WarningsExact identifier
application number: M007
Magnesium Citrate Saline Laxative - Lemon FlavorMAGNESIUM CITRATEUniversal Distribution Center LLCaa02c9af-22b8-4ec2-9e43-fe073f5e617b2026-03-11WarningsExact identifier
application number: M007
Magnesium Citrate Saline Laxative - Grape FlavorMAGNESIUM CITRATEUniversal Distribution Center LLC021ebb61-2466-4272-8f7d-b49cafd087542026-03-11WarningsExact identifier
application number: M007
Magnesium Citrate Saline Laxative - Cherry FlavorMAGNESIUM CITRATEUniversal Distribution Center LLC1f14411b-6833-40e6-b1a5-2b8c5bf709d32026-03-11WarningsExact identifier
application number: M007
CitromaMAGNESIUM CITRATEUpLift Brands, LLCf83ba007-734d-4910-87cb-02e45285e1612026-03-11Warnings, Adverse reactionsExact identifier
application number: M007
CitromaMAGNESIUM CITRATEUpLift Brands, LLC57e914fa-8fa2-4221-bb5f-534f0ea0aba72026-03-11Warnings, Adverse reactionsExact identifier
application number: M007
CitromaMAGNESIUM CITRATEUpLift Brands, LLCf28a9043-e0ee-4b38-95d9-d3f23d4006912026-03-11Warnings, Adverse reactionsExact identifier
application number: M007
Stool SoftenerDOCUSATE SODIUMAmerisource Bergen4caf0bcb-c1bf-0ae7-e063-6294a90a344b2026-03-10WarningsExact identifier
application number: M007
Stool Softener LaxativeDOCUSATE SODIUMWalgreens92df761b-da68-4ce9-b02a-a5a74fd6620e2026-03-10WarningsExact identifier
application number: M007
FleetGLYCERINC.B. Fleet Company, Inc.31778652-e60e-4098-8e90-3e4f56b5800c2026-03-06WarningsExact identifier
application number: M007
GlycerinGLYCERINBeijing Jingfeng Pharmaceutical (Shandong) Co., Ltd4c6094b7-c1ef-26a3-e063-6394a90af4cc2026-03-06WarningsExact identifier
application number: M007

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
312935sennosides 8.6 MG Oral TabletPSN4a9e1cbe-ffe4-462f-a86d-078a357dcf494
312935sennosides, USP 8.6 MG Oral TabletSCD4a9e1cbe-ffe4-462f-a86d-078a357dcf494
312935sennosides A and B 8.6 MG Oral TabletSY4a9e1cbe-ffe4-462f-a86d-078a357dcf494
312935sennosides 8.6 MG Oral TabletPSNdf3b431b-a1ad-91dd-e053-2995a90aa02f2
312935sennosides, USP 8.6 MG Oral TabletSCDdf3b431b-a1ad-91dd-e053-2995a90aa02f2
312935sennosides A and B 8.6 MG Oral TabletSYdf3b431b-a1ad-91dd-e053-2995a90aa02f2
312935sennosides 8.6 MG Oral TabletPSNd4ab04e4-b78a-4afc-aa16-d9dc8fb6cc101
312935sennosides, USP 8.6 MG Oral TabletSCDd4ab04e4-b78a-4afc-aa16-d9dc8fb6cc101
312935sennosides A and B 8.6 MG Oral TabletSYd4ab04e4-b78a-4afc-aa16-d9dc8fb6cc101

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0904-7252-6000904725260100 TABLET, FILM COATED in 1 BOTTLE (0904-7252-60) 2022-05-170000-00-00NoNoCurrent
0904-7252-610090472526110 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-7252-61) / 10 TABLET, FILM COATED in 1 BLISTER PACK10 blister pack2022-05-170000-00-00NoNoCurrent
0904-7252-80009047252801000 TABLET, FILM COATED in 1 BOTTLE (0904-7252-80) 2022-05-170000-00-00NoNoCurrent