Home NDC 30142-407 Stool Softener
Product NDC 30142-407
11-digit product format 301420407
Labeler code 30142
Product ID 30142-407_08649f4b-9276-f53f-e063-6394a90a023a
Type HUMAN OTC DRUG
Nonproprietary name Docusate Sodium
Dosage form CAPSULE, LIQUID FILLED
Route ORAL
Labeler KROGER COMPANY
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-03-01
Substance DOCUSATE SODIUM
Active strength 100 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 · 30 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 30142-407-01 D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 30142-407-01 D Discontinued by firm f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 30142-407-01 D Discontinued by firm 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 30142-407-01 D Discontinued by firm a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 30142-407-01 D Discontinued by firm cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 30142-407-01 D Discontinued by firm cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product D Discontinued by firm 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 30142-407-01 D Discontinued by firm 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 30142-407-01 D Discontinued by firm ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 30142-407-01 D Discontinued by firm 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 excluded product product D Discontinued by firm ad56d346431e…cc804d4bbf1e…2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 30142-407-01 D Discontinued by firm ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded product product D Discontinued by firm 367a005e9d99…383a685ebd0f…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 30142-407-01 D Discontinued by firm 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded product product D Discontinued by firm 557ba5c1ecfa…9c80585c8c6e…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 30142-407-01 D Discontinued by firm 557ba5c1ecfa…9c80585c8c6e…2022-08-30 03:57 UTC · source 2022-08-29 excluded product product I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 30142-407-01 I Inactivated by FDA fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded product product I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 30142-407-01 I Inactivated by FDA 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded product product I Inactivated by FDA bd6a592717d7…303034d00443…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 30142-407-01 I Inactivated by FDA bd6a592717d7…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 Stool Softener
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DOCUSATE SODIUM 100 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination F05Q2T2JA0 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1115005 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 30142-407-01 Stool Softener 100 in 1 BOTTLE CAPSULE, LIQUID FILLED 100 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 30142-407 STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [KROGER COMPANY] 4 Current NDC, Legacy NDC, 1 package rows 20231024_a1afaa71-7e8c-5a49-e053-2a95a90a4db0.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 31 of 42 · 829 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join HEB Stool Softener DOCUSATE SODIUM H E B afc54b8e-03d9-418c-9322-97d68f929031 2024-12-18 Warnings Exact identifier application number: M007 Foster and Thrive Gentle Laxative BISACODYL Strategic Sourcing Services LLC d03c2c42-d9d9-4b4b-a6ae-31d99425a228 2024-12-18 Warnings Exact identifier application number: M007 EX-LAX REGULAR STRENGTH CHOCOLATED STIMULANT LAXATIVE SENNOSIDES Haleon US Holdings LLC 59a26a7f-516f-4507-8dec-f40cf6cfaffc 2024-12-17 Warnings Exact identifier application number: M007 EX-LAX MAXIMUM STRENGTH STIMULANT LAXATIVE SENNOSIDES Haleon US Holdings LLC fb170340-c996-46cf-b165-84e136ba4151 2024-12-17 Warnings Exact identifier application number: M007 Senna Syrup NATURAL VEGETABLE LAXATIVE Bryant Ranch Prepack 7d1f092e-0e5b-4fed-a095-64449751582d 2024-12-16 Warnings Exact identifier application number: M007 Drug Mart Vegetable Laxative plus Stool Softener DOCUSATE SODIUM, SENNOSIDES Discount Drug Mart, Inc 1b6d59e8-112f-447f-b6e9-526b7d3bd01e 2024-12-13 Warnings Exact identifier application number: M007 Drug Mart Stool Softener plus Stimulant Laxative DOCUSATE SODIUM, SENNOSIDES Discount Drug Mart, Inc caf74258-922c-4b69-9bd6-57b3e918c7a6 2024-12-13 Warnings Exact identifier application number: M007 Docusate Sodium DOCUSATE SODIUM National Vitamin Company 0c66642c-82cb-42cd-82bb-5f95852cc5d1 2024-12-12 Warnings Exact identifier application number: M007 Foster and Thrive Fiber Laxative 147 CALCIUM POLYCARBOPHIL Strategic Sourcing Services LLC 88d341a6-28aa-4a20-bfed-1d5f3106c2ae 2024-12-12 Warnings Exact identifier application number: M007 Pedia-Lax SODIUM PHOSPHATE, DIBASIC AND SODIUM PHOSPHATE, MONOBASIC C.B. Fleet Company, Inc. f001a37d-8ed4-428b-af12-d6a83c22c127 2024-12-12 Warnings Exact identifier application number: M007 Careone Milk of magnesia Original Milk of Magnesia Original MAGNESIUM HYDROXIDE Retail Business Services, LLC. 13ffb00b-7c6f-47aa-bc82-2402d121a758 2024-12-11 Warnings Exact identifier application number: M007 CareOne Milk of Magnesia Cherry MAGNESIUM HYDROXIDE Retail Business Services, LLC. 1822f90d-f693-48d7-b338-a3f2ddfac4df 2024-12-11 Warnings Exact identifier application number: M007 MILK OF MAGNESIA MINT MAGNESIUM HYDROXIDE GOOD SENSE a951b6d0-9182-e1bc-e053-2a95a90a12b1 2024-12-09 Warnings Exact identifier application number: M007 milk of magnesia MAGNESIUM HYDROXIDE CVS Pharmacy b3a36251-edd6-4201-8da1-85d7a6ede173 2024-12-05 Warnings Exact identifier application number: M007 CITRUCEL METHYLCELLULOSE Haleon US Holdings LLC d27f6742-2dcc-451e-b803-6ffe183038ec 2024-12-05 Warnings Exact identifier application number: M007 Laxacin DOCUSATE SODIUM AND SENNOSIDES Alexso, Inc 0df9abaf-3997-4dde-8003-ae3d8d07cf39 2024-12-04 Warnings Exact identifier application number: M007 NuValu Epsom Salt MAGNESIUM SULFATE (HEPTAHYDRATE) J C SALES 9f3cf9a4-e5c0-41ff-9fd3-63efb0d973cd 2024-12-04 Warnings Exact identifier application number: M007 NuValu Epsom Salt MAGNESIUM SULFATE (HEPTAHYDRATE) J C SALES 5a503d8d-7899-4b1e-be6f-8e2a759af265 2024-12-04 Warnings Exact identifier application number: M007 SENNOSIDES SENNOSIDES CVS Pharmacy, Inc. 6dffc3f5-bae0-c436-e053-2991aa0a0f8b 2024-12-02 Warnings Exact identifier application number: M007 Pure and Gentle MINERAL OIL Medline Industries, LP 96d4cad5-0602-4c31-94ed-3117b4fd4a94 2024-11-26 Warnings Exact identifier application number: M007
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 30142-407-01 30142040701 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (30142-407-01) 2020-03-01 0000-00-00 No No Current