FDA.reportPublic FDA data

Senokot

Product NDC
67618-300
11-digit product format
676180300
Labeler code
67618
Product ID
67618-300_fd1324ab-ef79-42ee-b960-9b032a3a4af2
Type
HUMAN OTC DRUG
Nonproprietary name
standardized senna concentrate
Dosage form
TABLET
Route
ORAL
Labeler
Atlantis Consumer Healthcare, Inc.
Application
M007
Marketing category
OTC MONOGRAPH DRUG
Marketing start
1956-06-01
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
Senokot
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 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
312935Internal RxNorm lookup
404186Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
c18dd7fa-993b-440b-8cdd-f1551abb99caAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67618-300-10Senokot1 in 1 CARTONTABLET112
67618-300-10Senokot100 in 1 BOTTLE, PLASTICTABLET10012
67618-300-20Senokot10 in 1 BLISTER PACKTABLET1012
67618-300-20Senokot2 in 1 CARTONTABLET212
67618-300-50Senokot1 in 1 CARTONTABLET112
67618-300-50Senokot50 in 1 BOTTLE, PLASTICTABLET5012

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
67618-300-10EA - Each67618-3006d995b3f-8f49-4111-9050-f18f3f0be49912012-07-24
67618-300-11EA - Each67618-300550247ea-a7f8-4d6f-9cd9-b442d2c9f6d112012-07-24
67618-300-20EA - Each67618-300029befb9-b71d-41e1-8118-4fac1a66fc4412012-07-24
67618-300-40EA - Each67618-300147e5b3d-423c-45e9-8222-6f15b35fc06d12013-06-04
67618-300-50EA - Each67618-300e8768eff-fab6-4153-9fa7-44686f5e8f0512012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SENNOSIDESACTIVE INGREDIENT3FYP5M0IJXSENOKOT (STANDARDIZED SENNA CONCENTRATE) TABLET [PURDUE PRODUCTS LP]3
SENNOSIDESACTIVE MOIETY3FYP5M0IJXSENOKOT (STANDARDIZED SENNA CONCENTRATE) TABLET [PURDUE PRODUCTS LP]3
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUSINACTIVE INGREDIENTL11K75P92JSENOKOT (STANDARDIZED SENNA CONCENTRATE) TABLET [PURDUE PRODUCTS LP]3
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61USENOKOT (STANDARDIZED SENNA CONCENTRATE) TABLET [PURDUE PRODUCTS LP]3
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30SENOKOT (STANDARDIZED SENNA CONCENTRATE) TABLET [PURDUE PRODUCTS LP]3
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJSENOKOT (STANDARDIZED SENNA CONCENTRATE) TABLET [PURDUE PRODUCTS LP]3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67618-300SENOKOT (STANDARDIZED SENNA CONCENTRATE) TABLET [ATLANTIS CONSUMER HEALTHCARE, INC.]11Current NDC, Legacy NDC, 6 package rows20241228_c18dd7fa-993b-440b-8cdd-f1551abb99ca.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 9 of 42 · 833 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Stool Softener plus Stimulant LaxativeDOCUSATE SODIUM 50 MG AND SENNOSIDES 8.6 MGCARDINAL HEALTH, 110 DBA LEADER3fd9ba76-42f8-4ebe-b1bc-f81f08e702ce2026-03-06WarningsExact identifier
application number: M007
Magnesium CitrateEQUATE MAGNESIUM CITRATE ORAL SOLUTION - LEMONWalmart Inc.484d0421-59ea-3783-e063-6394a90af6332026-03-04WarningsExact identifier
application number: M007
Magnesium CitrateEQUATE MAGNESIUM CITRATE ORAL SOLUTION - CHERRYWalmart Inc.484c2586-9e6f-1ce5-e063-6394a90a0d812026-03-04WarningsExact identifier
application number: M007
Magnesium CitrateEQUATE MAGNESIUM CITRATE ORAL SOLUTION - GRAPEWalmart Inc.450ddcbd-7ccd-3670-e063-6294a90ac2bd2026-03-04WarningsExact identifier
application number: M007
Epsom SaltMAGNESIUM SULFATEAmazon.com Services LLC787ec4b0-c6c5-44ab-a53d-d6d25304f95e2026-03-03Warnings, Adverse reactionsExact identifier
application number: M007
citromaMAGNESIUM CITRATEOld East Main Co.3d0d63d7-640d-4e54-a6fd-6b265c79be092026-03-02Warnings, Adverse reactionsExact identifier
application number: M007
citromaMAGNESIUM CITRATEOld East Main Co.9b3b6cea-ab83-4b7c-a425-fd0ac7df426c2026-03-02Warnings, Adverse reactionsExact identifier
application number: M007
citromaMAGNESIUM CITRATEOld East Main Co.51ed515b-cc51-4ea1-b612-0904761350052026-03-02Warnings, Adverse reactionsExact identifier
application number: M007
Epsom SaltMAGNESIUM SULFATEOld East Main Co.a8af6e2d-0052-4fc9-a51a-c9dbeb1ad3f52026-03-02Warnings, Adverse reactionsExact identifier
application number: M007
citromaMAGNESIUM CITRATEChain Drug Marketing Association629c5817-13b7-4527-8998-93131ee3529e2026-02-27Warnings, Adverse reactionsExact identifier
application number: M007
citromaMAGNESIUM CITRATEChain Drug Marketing Association4df97cdc-e7a2-4350-8f95-a679cdcaff642026-02-27Warnings, Adverse reactionsExact identifier
application number: M007
citromaMAGNESIUM CITRATEChain Drug Marketing Association46b26b44-e065-4337-a071-fa036f8971402026-02-27Warnings, Adverse reactionsExact identifier
application number: M007
Magnesium CitrateMAGNESIUM CITRATEChain Drug Marketing Associationef163b24-ce92-4cbc-b45a-4fae3b5119492026-02-27Warnings, Adverse reactionsExact identifier
application number: M007
Epsom SaltMAGNESIUM SULFATEChain Drug Marketing Association4ee26633-8eb1-4c68-a768-20460404533a2026-02-27Warnings, Adverse reactionsExact identifier
application number: M007
Mineral OilMINERAL OILChain Drug Marketing Association3bfdad9c-ac58-4e92-b952-555e8a8351cd2026-02-27Warnings, Adverse reactionsExact identifier
application number: M007
Magnesium CitrateMAGNESIUM CITRATEThe Kroger Co.2bcab227-42b6-4bff-8363-f6800665755b2026-02-27Warnings, Adverse reactionsExact identifier
application number: M007
Magnesium CitrateMAGNESIUM CITRATEThe Kroger Co.a87dceb2-da73-4d3a-b87c-db2af10471bf2026-02-27Warnings, Adverse reactionsExact identifier
application number: M007
SunscreenAVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENEThe Kroger Co.3ae7e275-7bbc-4e62-b30f-013c40a899492026-02-27WarningsExact identifier
application number: M007
SennosidesSENNOSIDESCVS Pharmacy, Inc0b7736df-c7de-7d00-e063-6294a90aa57e2026-02-26WarningsExact identifier
application number: M007
DOCUSATE SODIUMDOCUSATE SODIUMPD-Rx Pharmaceuticals, Inc.5d300ea7-78eb-4e19-8333-1e42c73c4c542026-02-26WarningsExact identifier
application number: M007

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
312935sennosides 8.6 MG Oral TabletPSNc18dd7fa-993b-440b-8cdd-f1551abb99ca12
404186Senokot 8.6 MG Oral TabletPSNc18dd7fa-993b-440b-8cdd-f1551abb99ca12
404186sennosides, USP 8.6 MG Oral Tablet [Senokot]SBDc18dd7fa-993b-440b-8cdd-f1551abb99ca12
312935sennosides, USP 8.6 MG Oral TabletSCDc18dd7fa-993b-440b-8cdd-f1551abb99ca12
312935sennosides A and B 8.6 MG Oral TabletSYc18dd7fa-993b-440b-8cdd-f1551abb99ca12
404186Senokot 8.6 MG Oral TabletSYc18dd7fa-993b-440b-8cdd-f1551abb99ca12

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
67618-300-10676180300101 BOTTLE, PLASTIC in 1 CARTON (67618-300-10) / 100 TABLET in 1 BOTTLE, PLASTIC1956-06-010000-00-00NoNoCurrent
67618-300-20676180300202 BLISTER PACK in 1 CARTON (67618-300-20) / 10 TABLET in 1 BLISTER PACK2 blister pack1956-06-010000-00-00NoNoCurrent
67618-300-50676180300501 BOTTLE, PLASTIC in 1 CARTON (67618-300-50) / 50 TABLET in 1 BOTTLE, PLASTIC1956-06-010000-00-00NoNoCurrent