FDA.reportPublic FDA data

Senexon-S

Product NDC
0536-1247
11-digit product format
005361247
Labeler code
0536
Product ID
0536-1247_8ff24a4d-d516-4b17-a838-2a61f19686c5
Type
HUMAN OTC DRUG
Nonproprietary name
Docusate Sodium 50mg and Sennosides 8.6mg
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
RUGBY LABORATORIES
Application
M007
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-10-02
Substance
SENNOSIDES; DOCUSATE SODIUM
Active strength
8.6; 50 mg/1; 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
Senexon-S
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SENNOSIDES8.6 mg/1
DOCUSATE SODIUM50 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3FYP5M0IJXInternal UNII lookup
F05Q2T2JA0Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
998740Internal RxNorm lookup
1248013Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
2e758ff1-3083-4245-8f58-1c47b042bfddAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0536-1247-01Senexon-S100 in 1 BOTTLE, PLASTICTABLET, FILM COATED1003
0536-1247-10Senexon-S1000 in 1 BOTTLE, PLASTICTABLET, FILM COATED10003

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0536-1247-01EA - Each0536-1247d7ebf6c0-94d1-4058-a337-8a1c4cdc054c12019-11-12
0536-1247-10EA - Each0536-1247fc120350-f269-411f-a810-65f8d76772f012019-11-12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0536-1247SENEXON-S (DOCUSATE SODIUM 50MG AND SENNOSIDES 8.6MG) TABLET, FILM COATED [RUGBY LABORATORIES]3Current NDC, Legacy NDC, 2 package rows20241222_2e758ff1-3083-4245-8f58-1c47b042bfdd.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 5 of 42 · 833 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MILK OF MAGNESIA MINTMAGNESIUM HYDROXIDEPreferred Pharmaceuticals Inc.f8bba8cb-a111-4285-8bdb-2273a049c3bb2026-07-08WarningsExact identifier
application number: M007
DOCUSATE SODIUM, EXTRA STRENGTH 250 MGDOCUSATE SODIUMAdvanced Rx LLCfc8cf24e-8ca1-b3fb-e053-6294a90a7a502026-07-06WarningsExact identifier
application number: M007
Curewell Docusate Sodium LiquidDOCUSATE SODIUM.50MG/5MLRMT HEALTH LLC55903043-2a1d-0525-e063-6394a90ae1822026-07-01WarningsExact identifier
application number: M007
SennaSENNOSIDES 8.6 MG TABLETSAarkish Pharmaceuticals NJ Inc.564bc9a5-13b5-4cce-a349-6b2e122683ed2026-07-01WarningsExact identifier
application number: M007
Senna-SDOCUSATE SODIUM 50 MG SENNOSIDES 8.6 MGAarkish Pharmaceuticals NJ Inc.faca8f3e-d9eb-44c5-93ab-f59ed1c0f56f2026-07-01WarningsExact identifier
application number: M007
ENEMEEZDOCUSATE SODIUMQuest Products, LLC0b06445d-0839-497e-bdff-e0fe224a77382026-06-30WarningsExact identifier
application number: M007
ENEMEEZ PlusDOCUSATE SODIUM AND BENZOCAINEQuest Products, LLC1670ca59-7275-4ac6-bef4-674a7b24c7b32026-06-30WarningsExact identifier
application number: M007
Mineral oilMINERAL OILCVS Pharmacy, Inc.1183bcbc-51ec-e53a-e063-6394a90af0f22026-06-26Warnings, Adverse reactionsExact identifier
application number: M007
GlycerinGLYCERINBeijing Jingfeng Pharmaceutical (Shandong) Co., Ltd552d9018-cc7d-7e1a-e063-6294a90a33222026-06-26WarningsExact identifier
application number: M007
GlycerinGLYCERINBeijing Jingfeng Pharmaceutical (Shandong) Co., Ltd552e16b9-f46a-7838-e063-6394a90ab8aa2026-06-26WarningsExact identifier
application number: M007
Walgreens Gentle LaxativeBISACODYL SUPPOSITORYWalgreens20c43036-830b-0e1d-e063-6394a90adf5f2026-06-25WarningsExact identifier
application number: M007
Docusate SodiumDOCUSATE SODIUMAmerican Health Packagingbe7cab51-ce7e-465d-95db-083e69288cfd2026-06-25WarningsExact identifier
application number: M007
Epsom SaltMAGNESIUM SULFATEVi-Jon, LLCba490c22-19f0-4887-9509-bd3d32e0f5b12026-06-24Warnings, Adverse reactionsExact identifier
application number: M007
MILK OF MAGNESIAMAGNESIUM HYDROXIDEKROGER COMPANYa1b0c638-6c34-1b72-e053-2995a90acc852026-06-24WarningsExact identifier
application number: M007
Womens LaxativeWOMENS LAXTIVEAllegiant Health549a11d1-a096-4c22-96b4-2d4f54f460222026-06-24WarningsExact identifier
application number: M007
Magnesium CitrateMAGNESIUM CITRATEMeijer Distribution Incf4259fda-19d4-087e-e053-2995a90a70812026-06-22WarningsExact identifier
application number: M007
STOOL SOFTENERDOCUSATE SODIUMGeri-Care Pharmaceuticals, Corp3ec42148-6786-22f2-e054-00144ff8d46c2026-06-18WarningsExact identifier
application number: M007
GlycerinGLYCERIN SUPPOSITORYEverpharm LLC546347e5-841e-15ca-e063-6294a90a0c8b2026-06-16WarningsExact identifier
application number: M007
GlycerinGLYCERIN SUPPOSITORYEverpharm LLC5463f869-2b92-4551-e063-6394a90ad6f92026-06-16WarningsExact identifier
application number: M007
MINICA-SGLYCERINSato Pharmaceutical Co., Ltd.687902eb-e702-4e87-a0ce-9add05e3cbc12026-06-16WarningsExact identifier
application number: M007

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1248013Senexon-S 50 MG / 8.6 MG Oral TabletPSNc049ef78-cc16-4209-b553-60cead5c9a807
998740sennosides 8.6 MG / docusate sodium 50 MG Oral TabletPSNc049ef78-cc16-4209-b553-60cead5c9a807
1248013docusate sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet [Senexon S]SBDc049ef78-cc16-4209-b553-60cead5c9a807
998740docusate sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSCDc049ef78-cc16-4209-b553-60cead5c9a807
998740DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSYc049ef78-cc16-4209-b553-60cead5c9a807
1248013DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet [Senexon S]SYc049ef78-cc16-4209-b553-60cead5c9a807
1248013Senexon-S (docusate sodium 50 MG / sennosides, USP 8.6 MG) Oral TabletSYc049ef78-cc16-4209-b553-60cead5c9a807
1248013Senexon-S 50 MG / 8.6 MG Oral TabletPSN2e758ff1-3083-4245-8f58-1c47b042bfdd3
998740sennosides 8.6 MG / docusate sodium 50 MG Oral TabletPSN2e758ff1-3083-4245-8f58-1c47b042bfdd3
1248013docusate sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet [Senexon S]SBD2e758ff1-3083-4245-8f58-1c47b042bfdd3
998740docusate sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSCD2e758ff1-3083-4245-8f58-1c47b042bfdd3
998740DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSY2e758ff1-3083-4245-8f58-1c47b042bfdd3
1248013DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral Tablet [Senexon S]SY2e758ff1-3083-4245-8f58-1c47b042bfdd3
1248013Senexon-S (docusate sodium 50 MG / sennosides, USP 8.6 MG) Oral TabletSY2e758ff1-3083-4245-8f58-1c47b042bfdd3

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0536-1247-0100536124701100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0536-1247-01) 2019-10-020000-00-00NoNoCurrent
0536-1247-10005361247101000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0536-1247-10) 2019-10-020000-00-00NoNoCurrent