Home NDC 57896-206 EXTRA STRENGTH PAIN RELIEF
Product NDC 57896-206
11-digit product format 578960206
Labeler code 57896
Product ID 57896-206_4742eecd-767f-3e30-e063-6394a90a86ed
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form SUSPENSION
Route ORAL
Labeler GERI-CARE PHARMACEUTICAL CORP
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-06-01
Substance ACETAMINOPHEN
Active strength 500 mg/15mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2020-12-18 03:04 UTC · source 2020-12-17 excluded product product 57896-206 I Inactivated by FDA excluded / ndc_excluded.zip e2bbac7714bc…27bdfed8d636…2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 57896-206 57896-206-08 I Inactivated by FDA excluded / ndc_excluded.zip e2bbac7714bc…27bdfed8d636…
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 EXTRA STRENGTH PAIN RELIEF
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 500 mg/15mL
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 SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 57896-206-08 EXTRA STRENGTH PAIN RELIEF 237 mL in 1 BOTTLE SUSPENSION 237 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 57896-206 EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) SUSPENSION [GERI-CARE PHARMACEUTICAL CORP] 6 Current NDC, Legacy NDC, 1 package rows 20241222_99ec63ef-aa28-c2fb-e053-2a95a90a9f6d.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 49 of 79 · 1,579 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 57896-206-08 57896020608 237 mL in 1 BOTTLE (57896-206-08) 237 ml 2019-06-01 0000-00-00 No No Current