Home NDC 57896-201 Extra Strength Pain Relief
Product NDC 57896-201
11-digit product format 578960201
Labeler code 57896
Product ID 57896-201_4525a8f8-b8bd-c290-e063-6394a90a81d9
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
Marketing end 2026-11-30
Substance ACETAMINOPHEN
Active strength 500 mg/1
NDC exclude flag No
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 · 24 matching rows.
View current auxiliary records. · View the auxiliary file history.
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 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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 57896-201-01 Extra Strength Pain Relief 100 in 1 BOTTLE TABLET 100 7 57896-201-05 Extra Strength Pain Relief 50 in 1 BOTTLE TABLET 50 7 57896-201-10 Extra Strength Pain Relief 1000 in 1 BOTTLE TABLET 1000 7
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ACETAMINOPHEN ACTIVE INGREDIENT 362O9ITL9D EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) TABLET [BRYANT RANCH PREPACK] 1000 ACETAMINOPHEN ACTIVE MOIETY 362O9ITL9D EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) TABLET [BRYANT RANCH PREPACK] 1000 CROSPOVIDONE INACTIVE INGREDIENT 68401960MK EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) TABLET [BRYANT RANCH PREPACK] 1000 METHYLPARABEN INACTIVE INGREDIENT A2I8C7HI9T EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) TABLET [BRYANT RANCH PREPACK] 1000 POVIDONE INACTIVE INGREDIENT FZ989GH94E EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) TABLET [BRYANT RANCH PREPACK] 1000 PROPYLPARABEN INACTIVE INGREDIENT Z8IX2SC1OH EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) TABLET [BRYANT RANCH PREPACK] 1000 SODIUM STARCH GLYCOLATE TYPE A POTATO INACTIVE INGREDIENT 5856J3G2A2 EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) TABLET [BRYANT RANCH PREPACK] 1000 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) TABLET [BRYANT RANCH PREPACK] 1000 ACETAMINOPHEN ACTIVE INGREDIENT 362O9ITL9D ACETAMINOPHEN TABLET [KELTMAN PHARMACEUTICALS INC.] 2 ACETAMINOPHEN ACTIVE MOIETY 362O9ITL9D ACETAMINOPHEN TABLET [KELTMAN PHARMACEUTICALS INC.] 2 POVIDONE INACTIVE INGREDIENT FZ989GH94E ACETAMINOPHEN TABLET [KELTMAN PHARMACEUTICALS INC.] 2 SODIUM STARCH GLYCOLATE TYPE A POTATO INACTIVE INGREDIENT 5856J3G2A2 ACETAMINOPHEN TABLET [KELTMAN PHARMACEUTICALS INC.] 2 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ ACETAMINOPHEN TABLET [KELTMAN PHARMACEUTICALS INC.] 2 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP ACETAMINOPHEN TABLET [KELTMAN PHARMACEUTICALS INC.] 2 Acetaminophen ACTIVE INGREDIENT 362O9ITL9D EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) TABLET [GERI-CARE PHARMACEUTICAL CORP] 1 Acetaminophen ACTIVE INGREDIENT 362O9ITL9D ACETAMINOPHEN EXTRA STRENGTH (ACETAMINOPHEN) TABLET [PHYSICIANS TOTAL CARE, INC.] 1 Acetaminophen ACTIVE MOIETY 362O9ITL9D ACETAMINOPHEN EXTRA STRENGTH (ACETAMINOPHEN) TABLET [PHYSICIANS TOTAL CARE, INC.] 1 Acetaminophen ACTIVE MOIETY 362O9ITL9D EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) TABLET [GERI-CARE PHARMACEUTICAL CORP] 1 CROSPOVIDONE INACTIVE INGREDIENT 68401960MK ACETAMINOPHEN EXTRA STRENGTH (ACETAMINOPHEN) TABLET [PHYSICIANS TOTAL CARE, INC.] 1 METHYLPARABEN INACTIVE INGREDIENT A2I8C7HI9T ACETAMINOPHEN EXTRA STRENGTH (ACETAMINOPHEN) TABLET [PHYSICIANS TOTAL CARE, INC.] 1 POVIDONE INACTIVE INGREDIENT FZ989GH94E ACETAMINOPHEN EXTRA STRENGTH (ACETAMINOPHEN) TABLET [PHYSICIANS TOTAL CARE, INC.] 1 PROPYLPARABEN INACTIVE INGREDIENT Z8IX2SC1OH ACETAMINOPHEN EXTRA STRENGTH (ACETAMINOPHEN) TABLET [PHYSICIANS TOTAL CARE, INC.] 1 SODIUM STARCH GLYCOLATE TYPE A POTATO INACTIVE INGREDIENT 5856J3G2A2 ACETAMINOPHEN EXTRA STRENGTH (ACETAMINOPHEN) TABLET [PHYSICIANS TOTAL CARE, INC.] 1 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP ACETAMINOPHEN EXTRA STRENGTH (ACETAMINOPHEN) TABLET [PHYSICIANS TOTAL CARE, INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 57896-201 EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) TABLET [GERI-CARE PHARMACEUTICAL CORP] 6 Current NDC, Legacy NDC, 3 package rows 20240705_7570aaa2-3238-4cd3-b788-915caa970dba.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 9 of 83 · 1,657 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Dr Kids Pain and Fever ACETAMINOPHEN CalmCo LLC 5534a784-a7b1-5599-e063-6294a90a7961 2026-06-27 Warnings Exact identifier application number: M013 TYLENOL Extra Strength ACETAMINOPHEN Select Consumer Group LLC 529d3a51-a248-7c02-e063-6294a90a10ae 2026-06-27 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN Sportpharm LLC 830ffcaa-7ff8-4732-bc84-6a8c5e78722d 2026-06-25 Warnings Exact identifier application number: M013 Aspirin ASPIRIN Strategic Sourcing Services LLC ea2ef485-429e-4c63-ba7b-0a6b32892ad2 2026-06-25 Warnings Exact identifier application number: M013 Aspirin ASPIRIN Chain Drug Marketing Association, Inc. 055d8420-c189-4a9e-acdc-21627935c8eb 2026-06-25 Warnings Exact identifier application number: M013 Aspirin ASPIRIN Topco Associates, LLC 5f32cf74-dbea-496c-ba23-2040ea354f40 2026-06-25 Warnings Exact identifier application number: M013 Aspirin ASPIRIN Salado Sales, Inc. cf3139a5-e36e-48e3-bb6c-e102b0cec555 2026-06-25 Warnings Exact identifier application number: M013 Pain Relief Aspirin ASPIRIN Rite Aid Corporation bd69d3d2-5d38-47c6-98a6-124f7a43b8b0 2026-06-25 Warnings Exact identifier application number: M013 Aspirin Regular Strength ASPIRIN Walgreen Company 0b27c0fd-7ea8-4588-9169-5ad4e8df77ef 2026-06-25 Warnings Exact identifier application number: M013 Aspirin Low Dose ASPIRIN ARMY AND AIR FORCE EXCHANGE SERVICE e273ead7-7cbc-4fd5-a136-9d3558a35360 2026-06-24 Warnings Exact identifier application number: M013 Acetaminophen Regular Strength ACETAMINOPHEN CVS PHARMACY 5e35df92-6282-4ca6-902b-bb6bd326b487 2026-06-23 Warnings Exact identifier application number: M013 Pain Reliever ACETAMINOPHEN Orelli Inc. 4f9f1b4e-8bbb-49b9-8e6c-263edb2c084d 2026-06-22 Warnings Exact identifier application number: M013 Pain Relief Aspirin Chewable, Low Dose ASPIRIN Rite Aid Corporation 65cdce0f-be04-43ba-8c68-bdce7983cfa1 2026-06-22 Warnings Exact identifier application number: M013 Aspirin Regimen ASPIRIN Cardinal Health 110, LLC. DBA Leader 88f425df-712d-4911-824b-94085c7190b6 2026-06-19 Warnings Exact identifier application number: M013 Aspirin Low Dose ASPIRIN Meijer Distribution, Inc. 3716a7d4-a555-4e54-aa0a-7b8f3e32addb 2026-06-19 Warnings Exact identifier application number: M013 Pain Relief ACETAMINOPHEN DOLGENCORP, LLC acc94a3e-21b6-4375-9881-38cf9bab8692 2026-06-19 Warnings Exact identifier application number: M013 Aspirin Low Dose ASPIRIN L.N.K. International, Inc. 2f6ec676-3832-420e-be91-fce83f6586c8 2026-06-19 Warnings Exact identifier application number: M013 Headache Relief ACETAMINOPHEN, ASPIRIN, CAFFEINE DOLGENCORP, LLC e1e24d52-0b4d-400b-8181-e3f6ab75c4f6 2026-06-18 Warnings Exact identifier application number: M013 Neo-Lubrina Children ACETAMINOPHEN OPMX LLC 5476f4cf-4a5d-2287-e063-6394a90a5ed5 2026-06-17 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN Oncor Pharmaceuticals 4c396d0e-aa93-4f9e-b065-2e606f7f05cd 2026-06-17 Warnings Exact identifier application number: M013
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 57896-201-01 57896020101 100 TABLET in 1 BOTTLE (57896-201-01) 100 tablet 2012-01-01 0000-00-00 No No Current 57896-201-05 57896020105 50 TABLET in 1 BOTTLE (57896-201-05) 50 tablet 2012-01-01 0000-00-00 No No Current 57896-201-10 57896020110 1000 TABLET in 1 BOTTLE (57896-201-10) 1000 tablet 2012-01-01 2026-11-30 No No Current 57896-201-20 57896020120 1 TABLET in 1 BOTTLE (57896-201-20) 1 tablet 2022-11-01 0000-00-00 No No Current