Home NDC 56062-650 rapid release pain relief
Product NDC 56062-650
11-digit product format 560620650
Labeler code 56062
Product ID 56062-650_84c546cf-f9ec-4ef1-a97c-8cfe676d937b
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Publix Super Markets Inc
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2016-03-25
Substance ACETAMINOPHEN
Active strength 500 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 rapid release pain relief
Listing expiration 2026-12-31 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 198440 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 56062-650-71 rapid release pain relief 1 in 1 CARTON TABLET, FILM COATED 1 4 56062-650-71 rapid release pain relief 50 in 1 BOTTLE TABLET, FILM COATED 50 4 56062-650-78 rapid release pain relief 100 in 1 BOTTLE TABLET, FILM COATED 100 4 56062-650-78 rapid release pain relief 1 in 1 CARTON TABLET, FILM COATED 1 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 56062-650 RAPID RELEASE PAIN RELIEF (ACETAMINOPHEN) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC] 4 Current NDC, Legacy NDC, 4 package rows 20241027_d0b34133-d69d-47db-bf51-be942769c612.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 1 of 83 · 1,657 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 56062-650-71 56062065071 1 BOTTLE in 1 CARTON (56062-650-71) / 50 TABLET, FILM COATED in 1 BOTTLE 1 bottle 2016-03-25 0000-00-00 No No Current 56062-650-78 56062065078 1 BOTTLE in 1 CARTON (56062-650-78) / 100 TABLET, FILM COATED in 1 BOTTLE 1 bottle 2016-03-25 0000-00-00 No No Current