Home NDC 67618-120 Senokot
Product NDC 67618-120
11-digit product format 676180120
Labeler code 67618
Product ID 67618-120_8319c8b6-8d3f-416d-a864-39cb879df2da
Type HUMAN OTC DRUG
Nonproprietary name standardized senna concentrate
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Atlantis Consumer Healthcare, Inc.
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 1988-09-01
Substance SENNOSIDES
Active strength 17.2 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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
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 Senokot
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SENNOSIDES 17.2 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3FYP5M0IJX Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 602802 Internal RxNorm lookup 1039965 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 67618-120-06 Senokot 36 in 1 BOTTLE TABLET, FILM COATED 36 11 67618-120-12 Senokot 12 in 1 BLISTER PACK TABLET, FILM COATED 12 11 67618-120-12 Senokot 1 in 1 CARTON TABLET, FILM COATED 1 11 67618-120-36 Senokot 12 in 1 BLISTER PACK TABLET, FILM COATED 12 11 67618-120-36 Senokot 3 in 1 CELLO PACK TABLET, FILM COATED 3 11 67618-120-72 Senokot 1 in 1 CARTON TABLET, FILM COATED 1 11 67618-120-72 Senokot 2 in 1 PACKAGE TABLET, FILM COATED 2 11 67618-120-73 Senokot 72 in 1 BOTTLE TABLET, FILM COATED 72 11
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67618-120 SENOKOT (STANDARDIZED SENNA CONCENTRATE) TABLET, FILM COATED [ATLANTIS CONSUMER HEALTHCARE, INC.] 10 Current NDC, Legacy NDC, 8 package rows 20250419_d5bf67e5-82c6-edbf-e9ec-e027fdd47c84.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 20 of 42 · 829 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join up and up fiber therapy PSYLLIUM HUSK TARGET CORPORATION 956c48f8-c705-4a86-9866-c68a48ddeb6c 2025-11-05 Warnings Exact identifier application number: M007 CEO-TWO LAXATIVE Beutlich Pharmaceuticals, LLC 08670636-5795-4db0-e063-6294a90afa4b 2025-11-05 Warnings Exact identifier application number: M007 up and up gentle laxative BISACODYL Target Corporation 4a29dc2b-b68f-471b-a84e-4a5096aa3748 2025-11-04 Warnings Exact identifier application number: M007 Target Fiber Laxative PSYLLIUM HUSK TARGET CORPORATION a581116a-392d-4ac3-ae15-4318506a7b2a 2025-11-04 Warnings Exact identifier application number: M007 up and up fiber therapy CALCIUM POLYCARBOPHIL Target Corporation. e5473950-06f4-4ea4-975b-3ac94957e776 2025-11-04 Warnings Exact identifier application number: M007 up and up fiber therapy Natural Fiber PSYLLIUM HUSK Target Corporation f8b1c831-6fd0-4a58-9726-4e0f986c8084 2025-11-04 Warnings Exact identifier application number: M007 OneLAX BISACODYL AKRON PHARMA INC be4eeb4d-df29-45dc-94ff-933e52c8b6f6 2025-11-03 Warnings Exact identifier application number: M007 Gentle Stool Softener DOCUSATE SODIUM WALGREEN COMPANY 169b33f9-e559-47bf-bbba-c7eda4762c7f 2025-10-31 Warnings Exact identifier application number: M007 Senna S DOCUSATE SODIUM, SENNOSIDES Walgreens 765bfd9b-7a21-4315-9add-cf13007722d5 2025-10-31 Warnings Exact identifier application number: M007 Gentle Stool Softener DOCUSATE SODIUM WALGREEN COMPANY 71b15339-2585-4fae-8445-6fbb4f0a378e 2025-10-31 Warnings Exact identifier application number: M007 Stool Softener Laxative DOCUSATE SODIUM Major Pharmaceuticals 97561cd4-63d9-44c2-a3a3-ec668a09a4ed 2025-10-31 Warnings Exact identifier application number: M007 Fiber Caplets CALCIUM POLYCARBOPHIL SAFEWAY 08e2e8b0-90b3-48d6-a72a-40688c74771a 2025-10-29 Warnings Exact identifier application number: M007 Glycerin GLYCERIN Chain Drug Marketing Association Inc. 424d91f0-ecf9-6d9b-e063-6394a90a8006 2025-10-29 Warnings Exact identifier application number: M007 Publix Laxative Maximum Strength CALCIUM SENNOSIDES PUBLIX SUPER MARKETS, INC 11112859-ef1e-4b37-9915-ba4d06a3f198 2025-10-28 Warnings Exact identifier application number: M007 Publix Stimulant Laxative BISACODYL PUBLIX SUPER MARKETS, INC 02e596a7-b8e5-4f55-9bc6-6d17e0fabda7 2025-10-28 Warnings Exact identifier application number: M007 PUBLIX PSYLLIUM HUSK PUBLIX SUPER MARKETS, INC 55f98d3f-f282-4f19-b373-0b59640d274d 2025-10-28 Warnings Exact identifier application number: M007 PUBLIX CALCIUM POLYCARBOPHIL PUBLIX SUPER MARKETS, INC 02e3f4ce-8961-425c-98a9-3b9d66709ca5 2025-10-28 Warnings Exact identifier application number: M007 Publix Women Laxative BISACODYL PUBLIX SUPER MARKETS, INC 03eeca55-f239-4a01-a900-c1943f27a834 2025-10-28 Warnings Exact identifier application number: M007 Publix Fiber Therapy Orange Smooth PSYLLIUM HUSK PUBLIX SUPER MARKETS, INC b9c54c20-cd82-4627-9217-a66834db4799 2025-10-28 Warnings Exact identifier application number: M007 Publix Fiber Therapy Sugar Free PSYLLIUM HUSK PUBLIX SUPER MARKETS, INC ed3dc80a-a243-4013-9886-b148e3e3b662 2025-10-28 Warnings Exact identifier application number: M007
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 67618-120-06 67618012006 36 TABLET, FILM COATED in 1 BOTTLE (67618-120-06) 1988-09-01 0000-00-00 No No Current 67618-120-12 67618012012 1 BLISTER PACK in 1 CARTON (67618-120-12) / 12 TABLET, FILM COATED in 1 BLISTER PACK 1 blister pack 1988-09-01 0000-00-00 No No Current 67618-120-36 67618012036 3 BLISTER PACK in 1 CELLO PACK (67618-120-36) > 12 BLISTER PACK in 1 BLISTER PACK > 12 TABLET, FILM COATED in 1 BLISTER PACK 3 blister pack 1988-09-01 2023-01-01 No No Current 67618-120-72 67618012072 2 CARTON in 1 PACKAGE (67618-120-72) / 1 BOTTLE in 1 CARTON / 36 TABLET, FILM COATED in 1 BOTTLE 2 carton 2024-01-01 No No Current 67618-120-73 67618012073 72 TABLET, FILM COATED in 1 BOTTLE (67618-120-73) 2025-11-15 No No Current