FDA.reportPublic FDA data

Colon Detox

Product NDC
69729-151
11-digit product format
697290151
Labeler code
69729
Product ID
69729-151_11ee012a-51b2-9afd-e063-6294a90a2a5f
Type
HUMAN OTC DRUG
Nonproprietary name
Docusate sodium and Sennosides
Dosage form
TABLET
Route
ORAL
Labeler
OPMX LLC
Application
M007
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-11-16
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
Colon Detox
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
0a4d3265-080c-d2ed-e063-6394a90adbeeAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69729-151-60Colon Detox1 in 1 CARTONTABLET12
69729-151-60Colon Detox60 in 1 BOTTLETABLET602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69729-151COLON DETOX (DOCUSATE SODIUM AND SENNOSIDES) TABLET [OPMX LLC]2Current NDC, 2 package rows20240224_0a4d3265-080c-d2ed-e063-6394a90adbee.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 8 of 43 · 858 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Senna SyrupNATURAL VEGETABLE LAXATIVEBryant Ranch Prepack2c0d62e7-563b-46e4-9793-183e98e761a62026-03-25WarningsExact identifier
application number: M007
LaxomilBISACODYL 5MGPharmadel LLC3999935b-d8e8-52a6-e063-6294a90aa2a22026-03-20WarningsExact identifier
application number: M007
Laxative Enteric CoatedBISACODYL 5MGGrocery Outletc820e6a1-fa23-447a-9ee9-50a1bd617adb2026-03-19WarningsExact identifier
application number: M007
CITRUCELMETHYLCELLULOSEHaleon US Holdings LLC9d5f2244-a610-4d45-b6e8-e79bb17a558f2026-03-18WarningsExact identifier
application number: M007
Stool Softener LaxativeDOCUSATE SODIUMSafeway, Inc.f178b31d-4843-4b91-a0d5-ab5ade835dc22026-03-16WarningsExact identifier
application number: M007
Stool Softener LaxativeDOCUSATE SODIUMSafeway, Inc.12ab9c3c-1f4b-43cd-83ac-b5f80b1aa54c2026-03-13WarningsExact identifier
application number: M007
Castor OilCASTOR OILOld East Main Co.a1ca668a-3bf9-46a9-8a4f-5cb61547bb812026-03-12Warnings, Adverse reactionsExact identifier
application number: M007
Castor OilCASTOR OILVi-Jon, LLCb29775df-8470-4fe3-bee3-f0490ea6903f2026-03-12WarningsExact identifier
application number: M007
Castor OilCASTOR OILNice-Pak Products, LLCcc43d514-ee82-4314-99b2-c64380f987792026-03-12Warnings, Adverse reactionsExact identifier
application number: M007
FiberconCALCIUM POLYCARBOPHILFoundation Consumer Brands7992a4bb-5535-4a1d-867d-a99f7e0c1be72026-03-12WarningsExact identifier
application number: M007
Stool Softener LaxativeDOCUSATE SODIUMWalgreenscda27a9c-9175-4b07-9c0b-d8d8978829652026-03-12WarningsExact identifier
application number: M007
Magnesium Citrate Saline Laxative - Lemon FlavorMAGNESIUM CITRATEUniversal Distribution Center LLCaa02c9af-22b8-4ec2-9e43-fe073f5e617b2026-03-11WarningsExact identifier
application number: M007
Magnesium Citrate Saline Laxative - Grape FlavorMAGNESIUM CITRATEUniversal Distribution Center LLC021ebb61-2466-4272-8f7d-b49cafd087542026-03-11WarningsExact identifier
application number: M007
Magnesium Citrate Saline Laxative - Cherry FlavorMAGNESIUM CITRATEUniversal Distribution Center LLC1f14411b-6833-40e6-b1a5-2b8c5bf709d32026-03-11WarningsExact identifier
application number: M007
CitromaMAGNESIUM CITRATEUpLift Brands, LLCf83ba007-734d-4910-87cb-02e45285e1612026-03-11Warnings, Adverse reactionsExact identifier
application number: M007
CitromaMAGNESIUM CITRATEUpLift Brands, LLC57e914fa-8fa2-4221-bb5f-534f0ea0aba72026-03-11Warnings, Adverse reactionsExact identifier
application number: M007
CitromaMAGNESIUM CITRATEUpLift Brands, LLCf28a9043-e0ee-4b38-95d9-d3f23d4006912026-03-11Warnings, Adverse reactionsExact identifier
application number: M007
Stool SoftenerDOCUSATE SODIUMAmerisource Bergen4caf0bcb-c1bf-0ae7-e063-6294a90a344b2026-03-10WarningsExact identifier
application number: M007
Stool Softener LaxativeDOCUSATE SODIUMWalgreens92df761b-da68-4ce9-b02a-a5a74fd6620e2026-03-10WarningsExact identifier
application number: M007
FleetGLYCERINC.B. Fleet Company, Inc.31778652-e60e-4098-8e90-3e4f56b5800c2026-03-06WarningsExact identifier
application number: M007

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
998740sennosides 8.6 MG / docusate sodium 50 MG Oral TabletPSN0a4d3265-080c-d2ed-e063-6394a90adbee2
998740docusate sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSCD0a4d3265-080c-d2ed-e063-6394a90adbee2
998740DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSY0a4d3265-080c-d2ed-e063-6394a90adbee2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
69729-151-60697290151601 BOTTLE in 1 CARTON (69729-151-60) / 60 TABLET in 1 BOTTLE1 bottle2023-11-16NoNoCurrent