FDA.reportPublic FDA data

Sennosides, Docusate Sodium

Manufacturer
Contract Pharmacal Corp.
Effective date
2025-09-08
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:13:02

Label at a glance#

ProductSennosides, Docusate Sodium
Active ingredientDOCUSATE SODIUM, SENNOSIDES
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

iNova labeliNova label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
998740sennosides 8.6 MG / docusate sodium 50 MG Oral TabletPSN4
998740docusate sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSCD4
998740DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSY4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10267-5609-1Sennosides, Docusate Sodium10 in 1 BLISTER PACKTABLET, FILM COATED104
10267-5609-1Sennosides, Docusate Sodium1 in 1 CARTONTABLET, FILM COATED14
10267-5609-4Sennosides, Docusate Sodium1000 in 1 BOTTLETABLET, FILM COATED10004
10267-5609-5Sennosides, Docusate Sodium1 in 1 CARTONTABLET, FILM COATED14
10267-5609-5Sennosides, Docusate Sodium120 in 1 BOTTLETABLET, FILM COATED1204
10267-5609-6Sennosides, Docusate Sodium1 in 1 CARTONTABLET, FILM COATED14
10267-5609-6Sennosides, Docusate Sodium20 in 1 BOTTLETABLET, FILM COATED204
10267-5609-7Sennosides, Docusate Sodium60 in 1 BOTTLETABLET, FILM COATED604
10267-5609-7Sennosides, Docusate Sodium1 in 1 CARTONTABLET, FILM COATED14

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10267-560910267-5609-5, 10267-5609-7, 10267-5609-6, 10267-5609-1, 10267-5609-4

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
DOCUSATE SODIUMF05Q2T2JA0ACTIB
FD&C YELLOW NO. 6H77VEI93A8IACT
GUAR GUME89I1637KEIACT
LECITHIN, SOYBEAN1DI56QDM62IACT
MAGNESIUM STEARATE70097M6I30IACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
SENNOSIDES3FYP5M0IJXACTIB
POLYETHYLENE GLYCOL 40004R4HFI6D95IACT
POLYVINYL ALCOHOL, UNSPECIFIED532B59J990IACT
TALC7SEV7J4R1UIACT
SODIUM BENZOATEOJ245FE5EUIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
STARCH, CORNO8232NY3SJIACT
D&C YELLOW NO. 10 ALUMINUM LAKECQ3XH3DET6IACT
SILICON DIOXIDEETJ7Z6XBU4IACT

Source Document#

Source XML

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
3e4fb38b-542a-fab1-e063-6294a90af2abc3f2a947-6ca4-d099-e053-2a95a90ac76a2025-09-08Exact identifier
spl id: 3e4fb38b-542a-fab1-e063-6294a90af2ab
spl set id: c3f2a947-6ca4-d099-e053-2a95a90ac76a

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.