Stool Softener Laxative

Product NDC
63868-946
11-digit product format
638680946
Labeler code
63868
Product ID
63868-946_866fb276-b4fd-4634-b66e-38a6b29bb980
Type
HUMAN OTC DRUG
Nonproprietary name
docusate sodium and sennosides
Dosage form
TABLET
Route
ORAL
Labeler
QUALITY CHOICE (Chain Drug Marketing Association)
Application
M007
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2021-03-31
Substance
DOCUSATE SODIUM; SENNOSIDES
Active strength
50; 8.6 mg/1; mg/1
NDC exclude flag
No
Listing certified through
2027-12-31
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 Laxative
Listing expiration
2027-12-31

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
72f8e8d7-ee38-4bd3-8711-f11fded0cedeAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63868-946-01Stool Softener Laxative100 in 1 BOTTLE, PLASTICTABLET1005

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63868-946STOOL SOFTENER LAXATIVE (DOCUSATE SODIUM AND SENNOSIDES) TABLET [QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)]5Current NDC, Legacy NDC, 1 package rows20240502_72f8e8d7-ee38-4bd3-8711-f11fded0cede.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
998740sennosides 8.6 MG / docusate sodium 50 MG Oral TabletPSN72f8e8d7-ee38-4bd3-8711-f11fded0cede5
998740docusate sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSCD72f8e8d7-ee38-4bd3-8711-f11fded0cede5
998740DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSY72f8e8d7-ee38-4bd3-8711-f11fded0cede5

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63868-946-0163868094601100 TABLET in 1 BOTTLE, PLASTIC (63868-946-01) 100 tablet2021-03-310000-00-00NoNoCurrent