Home NDC 57896-102 Regular Strength Pain Relief
Product NDC 57896-102
11-digit product format 578960102
Labeler code 57896
Product ID 57896-102_2a93e117-2d7d-3bdd-e063-6294a90a4f28
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET
Route ORAL
Labeler Geri-Care Pharmaceutical Corp
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 1989-01-01
Substance ACETAMINOPHEN
Active strength 325 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 Regular Strength Pain Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 325 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 313782 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 57896-102-01 Regular Strength Pain Relief 100 in 1 BOTTLE TABLET 100 8 57896-102-05 Regular Strength Pain Relief 50 in 1 BOTTLE TABLET 50 8 57896-102-10 Regular Strength Pain Relief 1000 in 1 BOTTLE TABLET 1000 8 57896-102-20 Regular Strength Pain Relief 200 in 1 BOTTLE TABLET 200 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 57896-102 REGULAR STRENGTH PAIN RELIEF (ACETAMINOPHEN) TABLET [GERI-CARE PHARMACEUTICAL CORP] 8 Current NDC, Legacy NDC, 4 package rows 20250101_6158e954-32d8-4718-e053-2a91aa0a27f3.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 57896-102-01 57896010201 100 TABLET in 1 BOTTLE (57896-102-01) 100 tablet 2011-12-01 0000-00-00 No No Current 57896-102-05 57896010205 50 TABLET in 1 BOTTLE (57896-102-05) 50 tablet 2011-12-01 0000-00-00 No No Current 57896-102-10 57896010210 1000 TABLET in 1 BOTTLE (57896-102-10) 1000 tablet 2012-01-01 0000-00-00 No No Current 57896-102-20 57896010220 200 TABLET in 1 BOTTLE (57896-102-20) 200 tablet 2018-07-01 0000-00-00 No No Current