Home NDC 67618-310 Senokot-S
Product NDC 67618-310
11-digit product format 676180310
Labeler code 67618
Product ID 67618-310_e5dc8b86-705c-4b54-a9fe-20d02d62ad48
Type HUMAN OTC DRUG
Nonproprietary name standardized senna concentrate and docusate sodium
Dosage form TABLET
Route ORAL
Labeler Atlantis Consumer Healthcare, Inc.
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 1974-10-01
Substance SENNOSIDES; DOCUSATE SODIUM
Active strength 8.6; 50 mg/1; mg/1
NDC exclude flag No
Listing certified through 2027-12-31
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 Senokot-S
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SENNOSIDES 8.6 mg/1 DOCUSATE SODIUM 50 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 3FYP5M0IJX Internal UNII lookup F05Q2T2JA0 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 998740 Internal RxNorm lookup 1248015 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 67618-310 SENOKOT-S (STANDARDIZED SENNA CONCENTRATE AND DOCUSATE SODIUM) TABLET [ATLANTIS CONSUMER HEALTHCARE, INC.] 10 Current NDC, Legacy NDC, 6 package rows 20241228_c24cdc5e-62e0-41a6-8afb-512202a569f4.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 17 of 42 · 833 matching rows.
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 67618-310-01 67618031001 1 BLISTER PACK in 1 CARTON (67618-310-01) / 10 TABLET in 1 BLISTER PACK 1 blister pack 1974-10-01 0000-00-00 No No Current 67618-310-10 67618031010 1 BOTTLE, PLASTIC in 1 CARTON (67618-310-10) / 100 TABLET in 1 BOTTLE, PLASTIC 2026-09-30 No No Current 67618-310-30 67618031030 1 BOTTLE, PLASTIC in 1 CARTON (67618-310-30) / 30 TABLET in 1 BOTTLE, PLASTIC 1974-10-01 0000-00-00 No No Current 67618-310-60 67618031060 1 BOTTLE, PLASTIC in 1 CARTON (67618-310-60) / 60 TABLET in 1 BOTTLE, PLASTIC 1974-10-01 0000-00-00 No No Current