Senna S

Product NDC
21130-883
11-digit product format
211300883
Labeler code
21130
Product ID
21130-883_7645f18f-a849-4fc6-9661-0591c511bae6
Type
HUMAN OTC DRUG
Nonproprietary name
DOCUSATE SODIUM, SENNOSIDES
Dosage form
TABLET
Route
ORAL
Labeler
Safeway, Inc.
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-11-29
Marketing end
2026-12-29
Substance
DOCUSATE SODIUM; SENNOSIDES
Active strength
50; 8.6 mg/1; mg/1
NDC exclude flag
No
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 S

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
acb40b29-5fd5-4864-b6bf-4102e47a1683Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21130-883-30Senna S30 in 1 BOTTLE, PLASTICTABLET305
21130-883-30Senna S1 in 1 BOXTABLET15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21130-883SENNA S (DOCUSATE SODIUM, SENNOSIDES) TABLET [SAFEWAY, INC.]4Current NDC, Legacy NDC, 2 package rows20240810_acb40b29-5fd5-4864-b6bf-4102e47a1683.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 SDOCUSATE SODIUM, SENNOSIDESSafeway, Inc.acb40b29-5fd5-4864-b6bf-4102e47a16832026-01-05WarningsExact identifier
ndc (product): 21130-883

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
998740sennosides 8.6 MG / docusate sodium 50 MG Oral TabletPSNacb40b29-5fd5-4864-b6bf-4102e47a16835
998740docusate sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSCDacb40b29-5fd5-4864-b6bf-4102e47a16835
998740DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSYacb40b29-5fd5-4864-b6bf-4102e47a16835

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
21130-883-30211300883301 BOTTLE, PLASTIC in 1 BOX (21130-883-30) / 30 TABLET in 1 BOTTLE, PLASTIC2019-11-292026-12-29NoNoCurrent