Stool Softener

Product NDC
21130-902
11-digit product format
211300902
Labeler code
21130
Product ID
21130-902_255d1ce7-fe7d-8c00-e063-6394a90a7b4b
Type
HUMAN OTC DRUG
Nonproprietary name
Docusate sodium and Sennosides
Dosage form
TABLET
Route
ORAL
Labeler
BETTER LIVING BRANDS LLC.
Application
M007
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-09-30
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
Stool Softener
Listing expiration
2026-12-31

Active Ingredients#

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

Harmonized Identifiers#

Field, Values table
FieldValues
UniiF05Q2T2JA0, 3FYP5M0IJX
Rxcui998740

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21130-902-20Stool Softener200 in 1 BOTTLETABLET2002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21130-902STOOL SOFTENER (DOCUSATE SODIUM AND SENNOSIDES) TABLET [BETTER LIVING BRANDS LLC.]2Current NDC, 1 package rows20250110_f2c61c71-9a23-4bd3-e053-2a95a90ad460.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
998740sennosides 8.6 MG / docusate sodium 50 MG Oral TabletPSNf2c61c71-9a23-4bd3-e053-2a95a90ad4602
998740docusate sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSCDf2c61c71-9a23-4bd3-e053-2a95a90ad4602
998740DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSYf2c61c71-9a23-4bd3-e053-2a95a90ad4602

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
21130-902-2021130090220200 TABLET in 1 BOTTLE (21130-902-20) 200 tablet2024-09-30NoNoHistorical