FDA.reportPublic FDA data

Good Sense Pain Relief

Product NDC
0113-0484
11-digit product format
001130484
Labeler code
0113
Product ID
0113-0484_f89719ea-9f60-4389-9971-2f2bd2fd25df
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET
Route
ORAL
Labeler
L. Perrigo Company
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
1989-09-15
Substance
ACETAMINOPHEN
Active strength
500 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

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 · 5 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage0113-04840113-0484-02DDiscontinued by firm2026-10-05
excluded packagepackage0113-04840113-0484-52DDiscontinued by firm2026-10-05
excluded packagepackage0113-04840113-0484-76DDiscontinued by firm2026-10-05
excluded packagepackage0113-04840113-0484-82DDiscontinued by firm2026-10-05
excluded packagepackage0113-04840113-0484-85DDiscontinued by firm2026-10-05

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 · 47 matching rows.

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

Captured / source date, Package NDC, Snapshot table
Captured / source datePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-050113-0484-82d630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-050113-0484-85d630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-050113-0484-02d630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-050113-0484-52d630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-050113-0484-76d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-260113-0484-85f5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-260113-0484-02f5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-260113-0484-76f5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-260113-0484-82f5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-260113-0484-52f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-310113-0484-022ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-310113-0484-762ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-310113-0484-822ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-310113-0484-522ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-280113-0484-02a1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-280113-0484-76a1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-280113-0484-82a1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-280113-0484-52a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-210113-0484-02cfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-210113-0484-76cfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-210113-0484-82cfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-210113-0484-52cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-100113-0484-02cdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-100113-0484-76cdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-100113-0484-82cdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-100113-0484-52cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-310113-0484-02302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-310113-0484-76302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-310113-0484-82302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-310113-0484-52302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-200113-0484-02ed331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-200113-0484-76ed331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-200113-0484-82ed331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-200113-0484-52ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100113-0484-020efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-100113-0484-760efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-100113-0484-820efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-100113-0484-520efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-080113-0484-52ad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-080113-0484-02ad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-080113-0484-76ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-030113-0484-52367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-030113-0484-02367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-030113-0484-76367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-090113-0484-52557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-090113-0484-02557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-090113-0484-76557ba5c1ecfa…9c80585c8c6e…

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
Good Sense Pain Relief
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACETAMINOPHEN500 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
362O9ITL9DInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
198440Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
7f78028a-484b-48b3-a37a-1e0b055bbefcAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
75d4bef7-334c-4a95-abb5-bff9def24114Product name220260112
7dea7767-9f52-b60a-5435-33cb9cc28baeProduct name420250124
6338270f-96cb-0ecb-6fbb-0a9bc78001f4Product name720250116
11939cf5-0ea7-5df5-5127-00a7ce07fd7fProduct name520250115
0ca83774-3f79-b837-5d6f-c210102f3bc8Product name620250114
88300afc-e1c4-ad17-c80b-4957f1b809a5Product name520250113
4eddd6ca-259a-4c6c-a3a4-2025015ce043Product name720240611
16cde546-8deb-4df2-a072-dab5566ede95Product name120231003
20ab58de-c64a-4ec2-9210-3aa3fae2b66fProduct name120230808
a3631b20-02d1-41d7-8187-5e5e850b9e80Product name120230306
79e1734e-f721-4d46-978a-be382f771672Product name220230110
41b814f3-0166-1c53-c9ef-a0794c7daf9dProduct name320221110
a590be26-846c-8659-a5a1-fb25907965dcProduct name220221110
06cc817f-60e0-4473-8e6b-c44d11dc5af6Product name920220921
92ead9ae-674d-4eee-a492-c385d496891fProduct name320220308
103b151b-b17f-42ac-8624-3ef62f5e2975Product name220200507
b8497372-efe9-9dde-fa2d-59be9761aa64Product name920200428
20c8cafe-5cfc-44f8-a9be-a664f437f780Product name220200225
3a16d77a-e865-468a-aedf-6e58913c1c21Product name320190619
2a0c98e1-033f-4e0d-a0da-b5291ffbe880Product name120190320
00d531e4-b130-8c52-eaf9-826cbb6f15ddProduct name320190205
aa0f353d-f35e-62e4-4e1f-5b563f01c659Product name920190205
22d922aa-c443-d9f3-b23c-03b03a9ad31cProduct name720181220
377068df-225f-7318-a910-a1987cdfa361Product name320170608
23475c0b-a5b5-4fec-b97f-acca901eae6aProduct name120140718
105ef617-6fa4-6713-326f-72ec8a6b75a9Product name120140508
332e86c3-7875-ca6e-f934-2206d2b31996Product name120140508
3ed6b849-48b8-8899-c288-6eeb396123b6Product name120140508
47fd879b-91c5-e1e5-130f-29d082a871ecProduct name120140508
53855190-7124-8179-f018-e792f7c27f28Product name120140508
7dfac40f-a405-cd2e-7c06-3059ec0e1092Product name120140508
84fb0b3d-1d72-b672-bc70-2b676a23e7e0Product name120140508
96c5169b-5b9d-547d-bf22-d688d91866e4Product name120140508
b8e0daf1-fb81-290b-c0bf-873be19ef775Product name120140508
c35d1ac8-8885-2ee1-6c52-5a715b242c00Product name120140508
c8753a88-edde-8e17-a396-705537b52ceeProduct name120140508
cd4f9ae2-1343-ecd2-ce0f-97db0c2b51ceProduct name120140508
cf3a804d-0326-aa22-0142-c184b5657d85Product name120140508
d83c592c-dd97-4cbf-36ac-13da806684bdProduct name120140508
e01133ad-4dcd-c7f3-454b-2ff569ee160aProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0113-0484-00Good Sense Pain Relief200 in 1 BOTTLETABLET20011
0113-0484-02Good Sense Pain Relief550 in 1 BOTTLETABLET55011
0113-0484-52Good Sense Pain Relief10 in 1 VIALTABLET1011
0113-0484-62Good Sense Pain Relief24 in 1 BOTTLETABLET2411
0113-0484-62Good Sense Pain Relief1 in 1 CARTONTABLET111
0113-0484-71Good Sense Pain Relief50 in 1 BOTTLETABLET5011
0113-0484-71Good Sense Pain Relief1 in 1 CARTONTABLET111
0113-0484-76Good Sense Pain Relief1 in 1 CARTONTABLET111
0113-0484-76Good Sense Pain Relief120 in 1 BOTTLETABLET12011
0113-0484-78Good Sense Pain Relief1 in 1 CARTONTABLET111
0113-0484-78Good Sense Pain Relief100 in 1 BOTTLETABLET10011
0113-0484-82Good Sense Pain Relief2 in 1 CARTONTABLET211
0113-0484-82Good Sense Pain Relief100 in 1 BOTTLETABLET10011
0113-0484-85Good Sense Pain Relief1 in 1 CARTONTABLET111
0113-0484-85Good Sense Pain Relief250 in 1 BOTTLETABLET25011
0113-0484-90Good Sense Pain Relief500 in 1 BOTTLETABLET50011
0113-0484-93Good Sense Pain Relief1000 in 1 BOTTLETABLET100011

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0113-0484-52EA - Each0113-048479f3ec87-900a-4b9c-ac6e-dc83ed1feb4712016-12-07
0113-0484-62EA - Each0113-04845508b1e2-ffaf-4243-8620-b88a8f33369912012-07-24
0113-0484-71EA - Each0113-048426f199e8-ced4-4e7a-b2dd-bb5a5b80531f12012-07-24
0113-0484-76EA - Each0113-0484566a6878-e89a-4728-b1a2-f2d44d677c6512021-11-09
0113-0484-78EA - Each0113-0484ba09a6b5-91da-48ad-8411-2b400e44495c12012-07-24
0113-0484-82EA - Each0113-0484ab85e440-75c7-4390-ad3b-f74704ca908212021-11-09
0113-0484-85EA - Each0113-048414c4eece-9ba5-4626-932d-86c7d3d7fc5d12024-08-12
0113-0484-90EA - Each0113-0484c925f66e-f6cf-4280-8b71-388bc61f8bb512012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ACETAMINOPHENACTIVE INGREDIENT362O9ITL9DGOOD SENSE PAIN RELIEF (ACETAMINOPHEN) TABLET [L. PERRIGO COMPANY]5
ACETAMINOPHENACTIVE MOIETY362O9ITL9DGOOD SENSE PAIN RELIEF (ACETAMINOPHEN) TABLET [L. PERRIGO COMPANY]5
CARNAUBA WAXINACTIVE INGREDIENTR12CBM0EIZGOOD SENSE PAIN RELIEF (ACETAMINOPHEN) TABLET [L. PERRIGO COMPANY]5
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48GOOD SENSE PAIN RELIEF (ACETAMINOPHEN) TABLET [L. PERRIGO COMPANY]5
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOGOOD SENSE PAIN RELIEF (ACETAMINOPHEN) TABLET [L. PERRIGO COMPANY]5
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1AGOOD SENSE PAIN RELIEF (ACETAMINOPHEN) TABLET [L. PERRIGO COMPANY]5
POVIDONESINACTIVE INGREDIENTFZ989GH94EGOOD SENSE PAIN RELIEF (ACETAMINOPHEN) TABLET [L. PERRIGO COMPANY]5
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJGOOD SENSE PAIN RELIEF (ACETAMINOPHEN) TABLET [L. PERRIGO COMPANY]5
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65APGOOD SENSE PAIN RELIEF (ACETAMINOPHEN) TABLET [L. PERRIGO COMPANY]5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0113-0484GOOD SENSE PAIN RELIEF (ACETAMINOPHEN) TABLET [L. PERRIGO COMPANY]10Current NDC, Legacy NDC, 17 package rows20250112_7f78028a-484b-48b3-a37a-1e0b055bbefc.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 11 of 83 · 1,657 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sleep Aid Plus Pain ReliefACETAMINOPHEN, DIPHENHYDRAMINE HCLWalgreen Companye3929179-dad2-4f7e-a971-dbf80f2b5e1b2026-06-08WarningsExact identifier
application number: M013
LOW DOSE ASPIRINASPIRINPinnacle RX LLC53c11fb4-ba31-b5e5-e063-6394a90a9c1a2026-06-08WarningsExact identifier
application number: M013
Pain Reliever PMACETAMINOPHEN, DIPHENHYDRAMINE HCLWalgreen Company9655c38a-126b-459e-b31d-0aa33d9eb5222026-06-08WarningsExact identifier
application number: M013
Acetaminophen Regular StrengthACETAMINOPHENAurohealth LLCdce938f5-eeba-4a76-9261-2b1324c39a312026-06-08WarningsExact identifier
application number: M013
Childrens MapapACETAMINOPHENBryant Ranch Prepack69c90cc8-846a-42cf-933a-108671689e8f2026-06-05WarningsExact identifier
application number: M013
Aspirin Low DoseASPIRINRugby Laboratories63fcd93a-b1db-44ba-8f2b-055a7deb205d2026-06-04WarningsExact identifier
application number: M013
AcetaminophenACETAMINOPHENASCLEMED USA INC.707a9ea7-8f4e-4274-97bd-b8071a0ee06b2026-06-04WarningsExact identifier
application number: M013
Aspirin Adult low doseACETYLSALICYCLIC ACIDMedline Industries, LP6dd6501f-841c-4994-e053-2a91aa0ae2312026-06-04WarningsExact identifier
application number: M013
MedlineACETAMINOPHENMedline Industries, LPfc5e6f2a-e813-0666-e053-6394a90a66a72026-06-04WarningsExact identifier
application number: M013
MedlineACETAMINOPHENMedline Industries, LPfc5d92c2-4bbe-8ad1-e053-6294a90a65b62026-06-04WarningsExact identifier
application number: M013
acetaminophenACETAMINOPHENUnit Dose Solutions, Inc.537219ac-552a-a30e-e063-6394a90aa9d12026-06-04WarningsExact identifier
application number: M013
Pain Relief childrensACETAMINOPHENCVS PHARMACYff878f56-125a-4de7-b063-029f7030733d2026-06-04WarningsExact identifier
application number: M013
Back and Body Extra StrengthASPIRIN, CAFFEINECVS Pharmacy749e2be2-594a-4052-8fa5-45c9ade2d23c2026-06-03WarningsExact identifier
application number: M013
Childrens MapapACETAMINOPHENMajor Pharmaceuticalsefec6af2-8b26-47f6-88c8-b0a6d69a2d7d2026-06-03WarningsExact identifier
application number: M013
Acetaminophen PM Extra StrengthACETAMINOPHEN, DIPHENHYDRAMINE HCLUnited Natural Foods, Inc. dba UNFIae3114c3-8cfe-4b81-8ac7-c281fe68b4622026-06-03WarningsExact identifier
application number: M013
AcetaminophenACETAMINOPHENCOSTCO WHOLESALE CORPORATION3745aa18-a711-43ed-9bc4-1f087b3c53c02026-06-03WarningsExact identifier
application number: M013
TYLENOL Extra StrengthACETAMINOPHENKenvue Brands LLC3f653262-b931-7d42-e063-6394a90adddd2026-06-03WarningsExact identifier
application number: M013
Pain RelieverACETAMINOPHENWalgreen Company0b1bef50-7957-4ea1-9ae3-91f59ea2dbb42026-06-03WarningsExact identifier
application number: M013
Pain Reliever PMACETAMINOPHEN, DIPHENHYDRAMINE HCLWALMART INC.42310898-cf3a-4ffb-88bb-b8b84449156e2026-06-02WarningsExact identifier
application number: M013
PAIN RELIEFACETAMINOPHENMeijer, Inc.1319bab8-8f17-44fb-9d91-099b0ba38a8d2026-06-01WarningsExact identifier
application number: M013

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198440acetaminophen 500 MG Oral TabletPSN7f78028a-484b-48b3-a37a-1e0b055bbefc11
198440acetaminophen 500 MG Oral TabletSCD7f78028a-484b-48b3-a37a-1e0b055bbefc11
198440APAP 500 MG Oral TabletSY7f78028a-484b-48b3-a37a-1e0b055bbefc11
198440acetaminophen 500 MG Oral TabletPSN36708cac-c076-4514-bfa1-9db6918749003
198440acetaminophen 500 MG Oral TabletSCD36708cac-c076-4514-bfa1-9db6918749003
198440APAP 500 MG Oral TabletSY36708cac-c076-4514-bfa1-9db6918749003
198440acetaminophen 500 MG Oral TabletPSNd9bebb47-6ff4-4ddc-b48f-18f9423734842
198440acetaminophen 500 MG Oral TabletSCDd9bebb47-6ff4-4ddc-b48f-18f9423734842
198440APAP 500 MG Oral TabletSYd9bebb47-6ff4-4ddc-b48f-18f9423734842

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0113-0484-0000113048400200 TABLET in 1 BOTTLE (0113-0484-00) 200 tablet2025-08-14NoNoCurrent
0113-0484-0200113048402550 TABLET in 1 BOTTLE (0113-0484-02) 550 tablet1989-09-150000-00-00NoNoCurrent
0113-0484-520011304845210 TABLET in 1 VIAL (0113-0484-52) 10 tablet1989-09-150000-00-00NoNoCurrent
0113-0484-62001130484621 BOTTLE in 1 CARTON (0113-0484-62) / 24 TABLET in 1 BOTTLE1 bottle1989-09-150000-00-00NoNoCurrent
0113-0484-71001130484711 BOTTLE in 1 CARTON (0113-0484-71) / 50 TABLET in 1 BOTTLE1 bottle1989-09-150000-00-00NoNoCurrent
0113-0484-76001130484761 BOTTLE in 1 CARTON (0113-0484-76) > 120 TABLET in 1 BOTTLE1 bottle1989-09-150000-00-00NoNoCurrent
0113-0484-78001130484781 BOTTLE in 1 CARTON (0113-0484-78) / 100 TABLET in 1 BOTTLE1 bottle1989-09-150000-00-00NoNoCurrent
0113-0484-82001130484822 BOTTLE in 1 CARTON (0113-0484-82) > 100 TABLET in 1 BOTTLE2 bottle1989-09-150000-00-00NoNoCurrent
0113-0484-85001130484851 BOTTLE in 1 CARTON (0113-0484-85) > 250 TABLET in 1 BOTTLE1 bottle2022-03-230000-00-00NoNoCurrent
0113-0484-9000113048490500 TABLET in 1 BOTTLE (0113-0484-90) 500 tablet1989-09-150000-00-00NoNoCurrent
0113-0484-93001130484931000 TABLET in 1 BOTTLE (0113-0484-93) 1000 tablet2025-08-14NoNoCurrent