Home NDC 56062-192 pain relief
Product NDC 56062-192
11-digit product format 560620192
Labeler code 56062
Product ID 56062-192_2433b664-cded-f976-e063-6394a90a2975
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET, COATED
Route ORAL
Labeler PUBLIX SUPER MARKETS INC
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-05-01
Marketing end 2026-12-31
Substance ACETAMINOPHEN
Active strength 500 mg/1
NDC exclude flag No
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 pain relief 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 56062-192-01 pain relief 100 in 1 BOTTLE, PLASTIC TABLET, COATED 100 3 56062-192-01 pain relief 1 in 1 CARTON TABLET, COATED 1 3 56062-192-03 pain relief 1 in 1 CARTON TABLET, COATED 1 3 56062-192-03 pain relief 50 in 1 BOTTLE, PLASTIC TABLET, COATED 50 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 56062-192 PAIN RELIEF (ACETAMINOPHEN) TABLET, COATED [PUBLIX SUPER MARKETS INC] 3 Current NDC, Legacy NDC, 4 package rows 20241013_9e779cc6-4641-6132-e053-2a95a90a3493.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 2 of 83 · 1,657 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 56062-192-01 56062019201 1 BOTTLE, PLASTIC in 1 CARTON (56062-192-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC 2020-05-01 2026-12-31 No No Current 56062-192-03 56062019203 1 BOTTLE, PLASTIC in 1 CARTON (56062-192-03) > 50 TABLET, COATED in 1 BOTTLE, PLASTIC 2020-05-01 0000-00-00 No No Current