Home NDC 37808-244-10 Stool Softener
Product NDC 37808-244
Requested package NDC 37808-244-10
11-digit product format 378080244
Labeler code 37808
Product ID 37808-244_c69fcded-64ec-4434-9efb-11f9bde26eb4
Type HUMAN OTC DRUG
Nonproprietary name DOCUSATE SODIUM
Dosage form CAPSULE, LIQUID FILLED
Route ORAL
Labeler H E B
Application part334
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2014-03-28
Marketing end 2024-01-05
Substance DOCUSATE SODIUM
Active strength 100 mg/1
NDC exclude flag No
Listing certified through 0000-00-00
Current FDA listing Historical FDA.report record 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.
FDA-Initiated Inactive NDC Indexing# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded DOCUSATE SODIUM ACTIVE INGREDIENT F05Q2T2JA0 STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [H E B] 1 DOCUSATE ACTIVE MOIETY M7P27195AG STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [H E B] 1 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [H E B] 1 FD&C YELLOW NO. 6 INACTIVE INGREDIENT H77VEI93A8 STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [H E B] 1 GELATIN INACTIVE INGREDIENT 2G86QN327L STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [H E B] 1 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [H E B] 1 MEDIUM-CHAIN TRIGLYCERIDES INACTIVE INGREDIENT C9H2L21V7U STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [H E B] 1 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [H E B] 1 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [H E B] 1 SORBITAN INACTIVE INGREDIENT 6O92ICV9RU STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [H E B] 1 SORBITOL INACTIVE INGREDIENT 506T60A25R STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [H E B] 1 WATER INACTIVE INGREDIENT 059QF0KO0R STOOL SOFTENER (DOCUSATE SODIUM) CAPSULE, LIQUID FILLED [H E B] 1
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 37808-244-10 37808024410 1 BOTTLE, PLASTIC in 1 BOX (37808-244-10) > 100 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC 2014-03-28 2024-01-05 No No Current