FDA.reportPublic FDA data

SENNA-PLUS

Product NDC
71335-1674
Requested package NDC
71335-1674-9
11-digit product format
713351674
Labeler code
71335
Product ID
71335-1674_efcc90d6-8e49-47f4-a370-4bc1156cf742
Type
HUMAN OTC DRUG
Nonproprietary name
Sennosides and Docusate Sodium
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-05-01
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
SENNA-PLUS
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 · 1 matching rows.

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

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
7f8396e7-07f0-4c9c-be8a-9dc00139cb83Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71335-1674-1SENNA-PLUS30 in 1 BOTTLETABLET303
71335-1674-2SENNA-PLUS120 in 1 BOTTLETABLET1203
71335-1674-3SENNA-PLUS60 in 1 BOTTLETABLET603
71335-1674-4SENNA-PLUS90 in 1 BOTTLETABLET903
71335-1674-5SENNA-PLUS100 in 1 BOTTLETABLET1003
71335-1674-6SENNA-PLUS28 in 1 BOTTLETABLET283
71335-1674-7SENNA-PLUS56 in 1 BOTTLETABLET563
71335-1674-8SENNA-PLUS14 in 1 BOTTLETABLET143
71335-1674-9SENNA-PLUS20 in 1 BOTTLETABLET203

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71335-1674-2EA - Each71335-167486b018bc-d977-466b-901b-580249d5a13d12022-01-06
71335-1674-3EA - Each71335-1674c6138d0f-b193-47e5-900d-60d8de52bc3412022-03-09
71335-1674-5EA - Each71335-1674a3c81d97-7662-49bc-a1b9-13d1b25f519f12024-02-14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71335-1674SENNA-PLUS (SENNOSIDES AND DOCUSATE SODIUM) TABLET [BRYANT RANCH PREPACK]3Current NDC, Legacy NDC, 9 package rows20240410_7f8396e7-07f0-4c9c-be8a-9dc00139cb83.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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SENNA-PLUSSENNOSIDES AND DOCUSATE SODIUMBryant Ranch Prepack7f8396e7-07f0-4c9c-be8a-9dc00139cb832024-04-04WarningsExact identifier
ndc (package): 71335-1674-9
ndc (product): 71335-1674
ndc11 (package): 71335167409

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
998740sennosides 8.6 MG / docusate sodium 50 MG Oral TabletPSN7f8396e7-07f0-4c9c-be8a-9dc00139cb833
998740docusate sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSCD7f8396e7-07f0-4c9c-be8a-9dc00139cb833
998740DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSY7f8396e7-07f0-4c9c-be8a-9dc00139cb833

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1674-97133516740920 TABLET in 1 BOTTLE (71335-1674-9) 20 tablet2024-04-040000-00-00NoNoCurrent