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 5 of 79 · 1,579 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join SurviveX Travel Med MOD CONVENIENCE KIT Intent Brands LLC 522da86b-cfd7-dd20-e063-6394a90a51c6 2026-08-04 Warnings Exact identifier application number: M013 Extra Strength Pain Reliever mini softgels ACETAMINOPHEN 500 MG Shield Pharmaceuticals Corp 0ebb1902-6f8a-4bfb-9f2e-839d43bfca37 2026-08-04 Warnings Exact identifier application number: M013 Pain Reliever ACETAMINOPHEN Better Living Brands, LLC 743af02c-c762-42f5-8e01-2f62da15e04e 2026-08-04 Warnings Exact identifier application number: M013 Childrens Pain and Fever ACETAMINOPHEN Aurohealth LLC 9aea8aae-8702-4c93-8b07-69cd252f44d6 2026-08-03 Warnings Exact identifier application number: M013 Pain Relief Acetaminophen 325 mg ACETAMINOPHEN NUVICARE LLC 49a59b79-b8b4-4bf5-a403-0a14751efc55 2026-08-03 Warnings Exact identifier application number: M013 Childrens Pain and Fever ACETAMINOPHEN Aurohealth LLC d4e98f8e-f24c-4bdd-b750-fa4f877fb621 2026-07-31 Warnings Exact identifier application number: M013 KinderFarms Childrens Pain and Fever ACETAMINOPHEN KinderFarms, LLC 4f86419a-b940-a9c6-e063-6394a90a6a2b 2026-07-30 Warnings Exact identifier application number: M013 Acetaminophen Extra Strength ACETAMINOPHEN Family Dollar Stores, LLC 53f7a9c8-f40e-19b2-e063-6394a90a8695 2026-07-29 Warnings Exact identifier application number: M013 KinderFarms Infants Pain and Fever ACETAMINOPHEN KinderFarms, LLC 5468b149-8fac-8d6a-e063-6294a90a8c51 2026-07-29 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN CVS PHARMACY 258975d2-d8e8-407d-9804-df3b37a184e4 2026-07-29 Warnings Exact identifier application number: M013 Aspirin ASPIRIN Dolgencorp, Inc. (DOLLAR GENERAL & REXALL) 3ba0a9f2-062a-401e-82eb-54383a822366 2026-07-29 Warnings Exact identifier application number: M013 Aspirin 81mg Enteric Coated ASPIRIN Cardinal Health 107, LLC 277723db-3578-4842-92eb-2de325f87649 2026-07-28 Warnings Exact identifier application number: M013 Aspirin Low Dose Chewable ASPIRIN Better Living Brands, LLC 7afce7b4-c86a-43f7-83cf-15ebffba2f35 2026-07-28 Warnings Exact identifier application number: M013 Childrens Pain and Fever ACETAMINOPHEN Aurohealth LLC f818996c-36d2-4d3d-af3e-39949157edb9 2026-07-28 Warnings Exact identifier application number: M013 Pain Reliever PM Extra Strength ACETAMINOPHEN, DIPHENHYDRAMINE HCL L.N.K. International, Inc. 03b871e8-3e14-4ed8-a978-45129255b272 2026-07-27 Warnings Exact identifier application number: M013 Pain Relief Acetaminophen PM Extra Strength ACETAMINOPHEN AND DIPHENHYDRAMINE HCL Rite Aid Corporation 17d27771-a112-474f-9a58-29af0d7e1af3 2026-07-27 Warnings Exact identifier application number: M013 Infants TYLENOL ACETAMINOPHEN Kenvue Brands LLC 2143cc16-86db-4060-96da-5c228ae9207b 2026-07-24 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN Softgel Healthcare Pvt Ltd 352bb451-ffdc-411a-e063-6294a90a8cf5 2026-07-24 Warnings Exact identifier application number: M013 acetaminophen ACETAMINOPHEN NuCare Pharmaceuticals,Inc. fdb7331a-d029-8b2a-e053-6294a90adfcd 2026-07-24 Warnings Exact identifier application number: M013 Childrens Pain and Fever ACETAMINOPHEN Aurohealth LLC 5ada044e-50e8-4874-ac04-df5f1f9e735d 2026-07-24 Warnings Exact identifier application number: M013
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