Home NDC 41226-101-50 Extra Strength Mini Softgels Pain Reliever
Product NDC 41226-101
Requested package NDC 41226-101-50
11-digit product format 412260101
Labeler code 41226
Product ID 41226-101_4976f92d-e5df-290c-e063-6294a90afb17
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form CAPSULE, LIQUID FILLED
Route ORAL
Labeler THE KROGER CO
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-27
Substance ACETAMINOPHEN
Active strength 500 mg/1
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Extra Strength Mini Softgels Pain Reliever
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 500 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 362O9ITL9D Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 198439 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 41226-101-50 Extra Strength Mini Softgels Pain Reliever 50 in 1 BOTTLE CAPSULE, LIQUID FILLED 50 2
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 1 of 84 · 1,678 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 41226-101-50 41226010150 50 CAPSULE, LIQUID FILLED in 1 BOTTLE (41226-101-50) 2026-01-27 No No Current