Home NDC 0067-8142 EX-LAX
Product NDC 0067-8142
11-digit product format 000678142
Labeler code 0067
Product ID 0067-8142_2133e636-8bf8-4e31-b653-1ea9dc773e7e
Type HUMAN OTC DRUG
Nonproprietary name SENNOSIDES
Dosage form PILL
Route ORAL
Labeler Haleon US Holdings LLC
Application M007
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-07-01
Substance SENNOSIDES
Active strength 25 mg/1
NDC exclude flag No
Listing certified through 2026-12-31
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 EX-LAX
Brand name suffix MAXIMUM STRENGTH STIMULANT LAXATIVE
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SENNOSIDES 25 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 213073 Internal RxNorm lookup 251292 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0067-8142-01 EX-LAXMAXIMUM STRENGTH STIMULANT LAXATIVE 12 in 1 BLISTER PACK PILL 12 6 0067-8142-01 EX-LAXMAXIMUM STRENGTH STIMULANT LAXATIVE 2 in 1 CARTON PILL 2 6 0067-8142-02 EX-LAXMAXIMUM STRENGTH STIMULANT LAXATIVE 12 in 1 BLISTER PACK PILL 12 6 0067-8142-02 EX-LAXMAXIMUM STRENGTH STIMULANT LAXATIVE 4 in 1 CARTON PILL 4 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0067-8142 EX-LAX MAXIMUM STRENGTH STIMULANT LAXATIVE (SENNOSIDES) PILL [HALEON US HOLDINGS LLC] 6 Current NDC, Legacy NDC, 4 package rows 20241219_fb170340-c996-46cf-b165-84e136ba4151.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 0067-8142-01 00067814201 2 BLISTER PACK in 1 CARTON (0067-8142-01) / 12 PILL in 1 BLISTER PACK 2 blister pack 2017-07-01 0000-00-00 No No Current 0067-8142-02 00067814202 4 BLISTER PACK in 1 CARTON (0067-8142-02) / 12 PILL in 1 BLISTER PACK 4 blister pack 2017-07-01 0000-00-00 No No Current