FDA.reportPublic FDA data

Stool Softener

Product NDC
69842-887
Requested package NDC
69842-887-25
11-digit product format
698420887
Labeler code
69842
Product ID
69842-887_02721327-2031-433b-8a5e-5c5b526b577d
Type
HUMAN OTC DRUG
Nonproprietary name
docusate sodium and sennosides
Dosage form
TABLET
Route
ORAL
Labeler
CVS Pharmacy
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-02-01
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

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
Stool Softener
Brand name suffix
Plus Stimulant Laxative
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
1ed3a4d3-629c-4d70-ac03-d0db9f77a9c8Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69842-887-10Stool SoftenerPlus Stimulant Laxative100 in 1 BOTTLE, PLASTICTABLET10010
69842-887-10Stool SoftenerPlus Stimulant Laxative1 in 1 BOXTABLET110
69842-887-25Stool SoftenerPlus Stimulant Laxative250 in 1 BOTTLE, PLASTICTABLET25010
69842-887-40Stool SoftenerPlus Stimulant Laxative400 in 1 BOTTLE, PLASTICTABLET40010

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69842-887-10EA - Each69842-88751722957-df50-48b9-b417-be7d1b33b44c12024-08-12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-887STOOL SOFTENER PLUS STIMULANT LAXATIVE (DOCUSATE SODIUM AND SENNOSIDES) TABLET [CVS PHARMACY]8Current NDC, Legacy NDC, 4 package rows20240906_1ed3a4d3-629c-4d70-ac03-d0db9f77a9c8.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
Stool Softener Plus Stimulant LaxativeDOCUSATE SODIUM AND SENNOSIDESCVS Pharmacy1ed3a4d3-629c-4d70-ac03-d0db9f77a9c82025-11-06WarningsExact identifier
ndc (package): 69842-887-25
ndc (product): 69842-887
ndc11 (package): 69842088725

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
998740sennosides 8.6 MG / docusate sodium 50 MG Oral TabletPSN1ed3a4d3-629c-4d70-ac03-d0db9f77a9c810
998740docusate sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSCD1ed3a4d3-629c-4d70-ac03-d0db9f77a9c810
998740DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSY1ed3a4d3-629c-4d70-ac03-d0db9f77a9c810

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69842-887-2569842088725250 TABLET in 1 BOTTLE, PLASTIC (69842-887-25) 250 tablet2021-02-010000-00-00NoNoCurrent