FDA.reportPublic FDA data

Senna Plus

Product NDC
69842-883
11-digit product format
698420883
Labeler code
69842
Product ID
69842-883_bd224cac-866f-41a1-9aa8-fa6b09ad8a16
Type
HUMAN OTC DRUG
Nonproprietary name
DOCUSATE SODIUM, SENNOSIDES
Dosage form
TABLET
Route
ORAL
Labeler
CVS Pharmacy
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-12-27
Substance
DOCUSATE SODIUM; SENNOSIDES
Active strength
50; 8.6 mg/1; mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Senna Plus
Listing expiration
2026-12-31

Active Ingredients#

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

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
F05Q2T2JA0Internal UNII lookup
3FYP5M0IJXInternal 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
ae9d1672-9ade-4139-9126-5289b87fe574Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69842-883-18Senna Plus180 in 1 BOTTLE, PLASTICTABLET1807
69842-883-30Senna Plus1 in 1 BOXTABLET17
69842-883-30Senna Plus30 in 1 BOTTLE, PLASTICTABLET307

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-883SENNA PLUS (DOCUSATE SODIUM, SENNOSIDES) TABLET [CVS PHARMACY]5Current NDC, Legacy NDC, 3 package rows20240810_ae9d1672-9ade-4139-9126-5289b87fe574.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 PlusDOCUSATE SODIUM, SENNOSIDESCVS Pharmacyae9d1672-9ade-4139-9126-5289b87fe5742025-12-17WarningsExact identifier
ndc (product): 69842-883

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
998740sennosides 8.6 MG / docusate sodium 50 MG Oral TabletPSNae9d1672-9ade-4139-9126-5289b87fe5747
998740docusate sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSCDae9d1672-9ade-4139-9126-5289b87fe5747
998740DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSYae9d1672-9ade-4139-9126-5289b87fe5747

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69842-883-1869842088318180 TABLET in 1 BOTTLE, PLASTIC (69842-883-18) 180 tablet2019-12-270000-00-00NoNoCurrent
69842-883-30698420883301 BOTTLE, PLASTIC in 1 BOX (69842-883-30) / 30 TABLET in 1 BOTTLE, PLASTIC2019-12-270000-00-00NoNoCurrent