Signature Care Pain Relief

Product NDC
21130-111
Requested package NDC
21130-111-90
11-digit product format
211300111
Labeler code
21130
Product ID
21130-111_e36b10d6-75a1-413e-bd04-fca97d3376b9
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET
Route
ORAL
Labeler
Safeway
Application
part343
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2015-09-01
Marketing end
0000-00-00
Substance
ACETAMINOPHEN
Active strength
500 mg/1
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage21130-11121130-111-90DDiscontinued by firm2026-11-12

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 · 6 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21130-111-62Signature Care Pain Relief1 in 1 CARTONTABLET15
21130-111-62Signature Care Pain Relief24 in 1 BOTTLETABLET245
21130-111-71Signature Care Pain Relief50 in 1 BOTTLETABLET505
21130-111-71Signature Care Pain Relief1 in 1 CARTONTABLET15
21130-111-78Signature Care Pain Relief100 in 1 BOTTLETABLET1005
21130-111-78Signature Care Pain Relief1 in 1 CARTONTABLET15
21130-111-85Signature Care Pain Relief1 in 1 CARTONTABLET15
21130-111-85Signature Care Pain Relief250 in 1 BOTTLETABLET2505
21130-111-90Signature Care Pain Relief500 in 1 BOTTLETABLET5005

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21130-111SIGNATURE CARE PAIN RELIEF (ACETAMINOPHEN) TABLET [SAFEWAY]5Legacy NDC, 9 package rows20240924_917bcd06-6dc6-42b3-80b4-c6746b347261.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198440acetaminophen 500 MG Oral TabletPSN917bcd06-6dc6-42b3-80b4-c6746b3472615
198440acetaminophen 500 MG Oral TabletSCD917bcd06-6dc6-42b3-80b4-c6746b3472615
198440APAP 500 MG Oral TabletSY917bcd06-6dc6-42b3-80b4-c6746b3472615

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
21130-111-9021130011190500 TABLET in 1 BOTTLE (21130-111-90) 500 tablet2015-09-010000-00-00NoNoCurrent