FDA.reportPublic FDA data

Stimulant Laxative Plus Stool Softener

Product NDC
17856-1248
11-digit product format
178561248
Labeler code
17856
Product ID
17856-1248_38930b8a-9e76-2025-e063-6394a90a2478
Type
HUMAN OTC DRUG
Nonproprietary name
Docusate Sodium 50 mg and Sennosides 8.6 mg
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
ATLANTIC BIOLOGICALS CORP.
Application
M
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-10-22
Substance
SENNOSIDES; DOCUSATE SODIUM
Active strength
8.6; 50 mg/1; mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 8 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2024-03-11 06:39 UTC · source 2024-03-08excluded productproduct1332a3947898…d4bfe170f9cd…
2024-03-11 06:39 UTC · source 2024-03-08excluded packagepackage17856-1248-11332a3947898…d4bfe170f9cd…
2022-08-30 03:57 UTC · source 2022-08-29excluded productproductfb8cb913e6d1…eb8c232b6be0…
2022-08-30 03:57 UTC · source 2022-08-29excluded packagepackage17856-1248-1fb8cb913e6d1…eb8c232b6be0…
2022-04-09 23:13 UTC · source 2022-04-08excluded productproduct86f5da6cb304…a595104c45d7…
2022-04-09 23:13 UTC · source 2022-04-08excluded packagepackage17856-1248-186f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01excluded productproductbd6a592717d7…303034d00443…
2022-04-04 05:40 UTC · source 2022-04-01excluded packagepackage17856-1248-1bd6a592717d7…303034d00443…

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
Stimulant Laxative Plus Stool Softener
Listing expiration
2026-12-31

Active Ingredients#

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

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3FYP5M0IJXInternal UNII lookup
F05Q2T2JA0Internal 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
4c02fcec-6bb7-4497-96c5-0d809209dd17Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
17856-1248-12024-05-09C16284748780-1d6a99b39-7535-a426-e053-dadaa90af4c2Drug Facts
17856-1248-12022-01-28C16284748780-1d6a99b39-7535-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17856-1248-1Stimulant Laxative Plus Stool Softener1 in 1 POUCHTABLET, FILM COATED13
17856-1248-1Stimulant Laxative Plus Stool Softener100 in 1 BOX, UNIT-DOSETABLET, FILM COATED1003

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
17856-1248-1EA - Each17856-1248549c3ebe-ea2f-42b6-a099-5857dd18c05d12021-07-15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17856-1248STIMULANT LAXATIVE PLUS STOOL SOFTENER (DOCUSATE SODIUM 50 MG AND SENNOSIDES 8.6 MG) TABLET, FILM COATED [ATLANTIC BIOLOGICALS CORP.]2Current NDC, Legacy NDC, 2 package rows20240511_4c02fcec-6bb7-4497-96c5-0d809209dd17.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 3 of 6 · 111 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
THERASTAT, CHERRYCHERRY COUGH DROPSHART Healthe3fdd1de-8f28-4063-a590-6c44507dead12025-12-23WarningsExact identifier
application number: M
Crystal Clean Antibacterial HandSoapBENZALKONIUM CHLORIDEChemcor Chemical Corporation308969b5-5ab2-44ef-ac70-9518a5dfbee22025-12-22WarningsExact identifier
application number: M
Foaming Antibacterial HandsoapBENZALKONIUM CHLORIDEChemcor Chemical Corporationeed9b007-0dc1-4954-891f-a7a042e763aa2025-12-22WarningsExact identifier
application number: M
Antibacterial HandsoapBENZALKONIUM CHLORIDEChemcor Chemical Corporation1022be5e-d515-4a06-bf2b-65774ec29a0b2025-12-22WarningsExact identifier
application number: M
Healthy Hands Foaming Hand SanitizerN/AMaintex746650b8-74b7-43f0-bdfc-62a68764f9362025-12-22WarningsExact identifier
application number: M
Chemcor Chemical Foaming Hand SanitizerBENZALKONIUM CHLORIDEChemcor Chemical Corporation5c9d90c1-0381-4237-9529-398fa51b3ab42025-12-22WarningsExact identifier
application number: M
Fresh HandsBENZALKONIUM CHLORIDEMaintexe174083a-8820-4fa7-8cc2-0a2c86f27cd62025-12-22WarningsExact identifier
application number: M
Aluminum HydroxideALUMINUM HYDROXIDEATLANTIC BIOLOGICALS CORP.60a54d4e-89c2-4329-86bf-a288527f37b52025-12-15WarningsExact identifier
application number: M
MAX relief juniorACETAMINOPHENATLANTIC BIOLOGICALS CORP.ff1f6f82-0c7c-4e3f-a2bd-3185e16fa7702025-12-10WarningsExact identifier
application number: M
Health One Pain Relief Cream with Lidocaine 4%PAIN RELIEF CREAM WITH LIDOCAINE 4%ONE2ZEE LIMITED LIABILITY COMPANY46a2276f-9da0-4e41-92f0-b17c302c72222025-12-03WarningsExact identifier
application number: M
Health One Deep Relieving GelDEEP RELIEVING GELONE2ZEE LIMITED LIABILITY COMPANY41d837f1-09e4-4ce3-8c1a-725c2147c7de2025-12-03WarningsExact identifier
application number: M
Hand SanitizerANTISEPTIC GELHART Health87fcd27f-e4bf-4ae9-ad2e-b9b11ac554cc2025-12-02WarningsExact identifier
application number: M
AB 3000BENZALKONIUM CHLORIDEChemco892c8911-9f1a-4c0c-9106-6d9a90d577a92025-11-06WarningsExact identifier
application number: M
Strike Bac Antibacterial HandBENZALKONIUM CHLORIDEGenlabs Corporation4014aa67-8016-40c5-88ec-daec9dba4f452025-11-06WarningsExact identifier
application number: M
Metro Antimicrobial HandBENZALKONIUM CHLORIDEMaintexa84d83dd-2445-4d0f-b763-2c69e8248cf92025-11-06WarningsExact identifier
application number: M
Butler Clean HandsBENZALKONIUM CHLORIDEMaintex3fd526a8-d197-4a12-b51b-165e706720a72025-11-06WarningsExact identifier
application number: M
First Street Dishwashing Concentrate and Antibacterial HandBENZALKONIUM CHLORIDEAmerifoods Trading Companyfc81ef1a-db55-411e-8b25-7dd59dd38eda2025-11-06WarningsExact identifier
application number: M
Champion Ultra CleanBENZALKONIUM CHLORIDEMaintex47426f67-af14-4b42-8ada-11b3648269492025-11-06WarningsExact identifier
application number: M
Premium Protection Antibacterial HandBENZALKONIUM CHLORIDEMaintex53bd6860-dde3-4525-ba1b-50f69be09abc2025-11-06WarningsExact identifier
application number: M
Hy-G-ClenzBENZALKONIUM CHLORIDEMicronova Manufacturing, Inc.ce96634e-1ce8-4244-b317-8e1da249de832025-11-06WarningsExact identifier
application number: M

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
998740sennosides 8.6 MG / docusate sodium 50 MG Oral TabletPSN4c02fcec-6bb7-4497-96c5-0d809209dd173
998740docusate sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSCD4c02fcec-6bb7-4497-96c5-0d809209dd173
998740DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSY4c02fcec-6bb7-4497-96c5-0d809209dd173

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
17856-1248-117856124801100 POUCH in 1 BOX, UNIT-DOSE (17856-1248-1) / 1 TABLET, FILM COATED in 1 POUCH100 pouch2024-05-090000-00-00NoNoCurrent