Pain Relief

Product NDC
36800-770
11-digit product format
368000770
Labeler code
36800
Product ID
36800-770_286014c1-2183-fc25-e063-6394a90aa15e
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET, COATED
Route
ORAL
Labeler
TopCo Associates LLC
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2014-03-31
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 · 4 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage36800-77036800-770-01DDiscontinued by firm2026-10-16
excluded packagepackage36800-77036800-770-03DDiscontinued by firm2026-10-16
excluded packagepackage36800-77036800-770-05DDiscontinued by firm2026-10-16
excluded packagepackage36800-77036800-770-12DDiscontinued by firm2026-10-16

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 · 48 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 2025-12-0536800-770-01d630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-0536800-770-03d630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-0536800-770-12d630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-0536800-770-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-2636800-770-01f5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-2636800-770-03f5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-2636800-770-12f5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-2636800-770-05f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-3136800-770-012ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-3136800-770-032ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-3136800-770-122ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-3136800-770-052ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-2836800-770-01a1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-2836800-770-03a1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-2836800-770-12a1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-2836800-770-05a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-2136800-770-01cfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-2136800-770-03cfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-2136800-770-12cfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-2136800-770-05cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-1036800-770-01cdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-1036800-770-03cdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-1036800-770-12cdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-1036800-770-05cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-3136800-770-01302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-3136800-770-03302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-3136800-770-12302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-3136800-770-05302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-2036800-770-01ed331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-2036800-770-03ed331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-2036800-770-12ed331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-2036800-770-05ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-1036800-770-010efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-1036800-770-030efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-1036800-770-120efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-1036800-770-050efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-0836800-770-03ad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-0836800-770-05ad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-0836800-770-12ad56d346431e…cc804d4bbf1e…
2024-11-09 02:27 UTC · source 2024-11-0836800-770-01ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-0336800-770-03367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-0336800-770-05367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-0336800-770-12367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-0336800-770-01367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-0936800-770-03557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-0936800-770-05557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-0936800-770-12557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-0936800-770-01557ba5c1ecfa…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
Pain Relief
Brand name suffix
Extra Strength
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
ecd6df7e-e7e2-446b-85ef-25971281fe31Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
36800-770-01Pain ReliefExtra Strength1 in 1 CARTONTABLET, COATED17
36800-770-01Pain ReliefExtra Strength24 in 1 BOTTLE, PLASTICTABLET, COATED247
36800-770-02Pain ReliefExtra Strength1 in 1 CARTONTABLET, COATED17
36800-770-02Pain ReliefExtra Strength50 in 1 BOTTLE, PLASTICTABLET, COATED507
36800-770-03Pain ReliefExtra Strength100 in 1 BOTTLE, PLASTICTABLET, COATED1007
36800-770-03Pain ReliefExtra Strength1 in 1 CARTONTABLET, COATED17
36800-770-05Pain ReliefExtra Strength1 in 1 CARTONTABLET, COATED17
36800-770-05Pain ReliefExtra Strength225 in 1 BOTTLE, PLASTICTABLET, COATED2257
36800-770-12Pain ReliefExtra Strength400 in 1 BOTTLE, PLASTICTABLET, COATED4007

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
36800-770PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET, COATED [TOPCO ASSOCIATES LLC]7Current NDC, Legacy NDC, 9 package rows20241206_ecd6df7e-e7e2-446b-85ef-25971281fe31.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 71 of 79 · 1,579 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Dye Free Infants Pain and FeverACETAMINOPHENWALGREENS0b1d88d8-56ff-9e9d-e063-6394a90a015c2024-04-09WarningsExact identifier
application number: M013
Headache Relief Extra StrengthACETAMINOPHEN, ASPIRIN, CAFFEINEH E B4d572228-3141-4539-9c3d-2fd06e94eee32024-04-09WarningsExact identifier
application number: M013
Excedrin Extra Strength Pain RelieverACETAMINOPHEN, ASPIRIN (NSAID), AND CAFFEINEHaleon US Holdings LLC1b5ff867-5442-4cf8-bd1e-530093cc88f82024-04-05WarningsExact identifier
application number: M013
Excedrin Extra Strength Pain RelieverACETAMINOPHEN, ASPIRIN (NSAID), AND CAFFEINEHaleon US Holdings LLC0faa3592-4d56-4645-9a0e-066e0bdfebb62024-04-05WarningsExact identifier
application number: M013
Pain Relief Childrens Dye FreeACETAMINOPHENH E B3f9beeeb-5e27-4b81-a647-20e65f0e9fc92024-04-03WarningsExact identifier
application number: M013
Low Dose AspirinASPIRINH E Bedb321dd-e5cb-4031-a8a8-efce9e86fe162024-04-03WarningsExact identifier
application number: M013
Childrens Pain ReliefACETAMINOPHENH E Ba0c0277e-50aa-4328-8f93-ab20c6176b2b2024-04-03WarningsExact identifier
application number: M013
Regular Strength Enteric coated aspirinASPIRINBryant Ranch Prepackbda805ab-7f37-405d-a144-4e06ad9a29a12024-04-03WarningsExact identifier
application number: M013
Headache Relief Extra StrengthACETAMINOPHEN, ASPIRIN, CAFFEINEFamily Dollar (FAMILY WELLNESS)650cb15e-c448-4df3-b0f8-4398be05d8412024-03-27WarningsExact identifier
application number: M013
Good Sense Effervescent Pain ReliefASPIRINPerrigo Direct, Inc.103027a7-2f0e-8d8c-e063-6294a90aedc72024-03-26WarningsExact identifier
application number: M013
rugby infants acetaminophenACETAMINOPHENRugby Laboratories8aa9ac68-ca61-4163-a876-52034138c1ea2024-03-25WarningsExact identifier
application number: M013
Equate Pain Reliever Acetaminophen for Adults 250 mgACETAMINOPHENWalmart Inc08a18481-f029-f01f-e063-6294a90aac652024-03-21WarningsExact identifier
application number: M013
Equate Pain Reliever Acetaminophen for Adults 250 mgACETAMINOPHENWalmart Inc0d106fa2-2a77-deb2-e063-6394a90a2dac2024-03-21WarningsExact identifier
application number: M013
Pain Relief Extra StrengthACETAMINOPHENEQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)872c5220-a379-4dc1-b99c-f11ebb82db352024-03-19WarningsExact identifier
application number: M013
Pain Reliever PM Extra StrengthACETAMINOPHEN, DIPHENHYDRAMINE HCLEQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)79886972-47a4-44c5-a131-1a691a3281032024-03-19WarningsExact identifier
application number: M013
Headache Relief Extra StrengthACETAMINOPHEN, ASPIRIN, CAFFEINEDolgencorp, Inc. (DOLLAR GENERAL & REXALL)5ffcc78d-9163-4cb4-8811-ae9f0142806a2024-03-18WarningsExact identifier
application number: M013
ASPIRIN LOW DOSE CHEWABLE ORANGE PAIN RELIEVERASPIRIN LOW DOSE CHEWABLE ORANGE PAIN RELIEVERHF Acquisition Co LLC, DBA HealthFirst13e621dc-b2b4-98fd-e063-6394a90acc752024-03-17WarningsExact identifier
application number: M013
Childrens Pain and FeverACETAMINOPHENCVS PHARMACY, INC097a9c98-a092-400d-9600-6797b0b9a50c2024-03-15WarningsExact identifier
application number: M013
Excedrin PM Triple Action Caplets and Excedrin Tension HeadacheACETAMINOPHEN, ASPIRIN (NSAID), CAFFEINE, AND DIPHENHYDRAMINE CITRATEHaleon US Holdings LLC978a9d27-6d41-42cb-a193-11314923d2ac2024-03-14WarningsExact identifier
application number: M013
Excedrin PM Triple Action CapletsACETAMINOPHEN, ASPIRIN (NSAID) AND DIPHENHYDRAMINE CITRATEHaleon US Holdings LLCb3812d27-40af-40d7-864a-dfa4ae34cb9e2024-03-14WarningsExact identifier
application number: M013

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198440acetaminophen 500 MG Oral TabletPSNecd6df7e-e7e2-446b-85ef-25971281fe317
198440acetaminophen 500 MG Oral TabletSCDecd6df7e-e7e2-446b-85ef-25971281fe317
198440APAP 500 MG Oral TabletSYecd6df7e-e7e2-446b-85ef-25971281fe317

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
36800-770-01368000770011 BOTTLE, PLASTIC in 1 CARTON (36800-770-01) > 24 TABLET, COATED in 1 BOTTLE, PLASTIC2014-03-310000-00-00NoNoCurrent
36800-770-02368000770021 BOTTLE, PLASTIC in 1 CARTON (36800-770-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC2014-03-310000-00-00NoNoCurrent
36800-770-03368000770031 BOTTLE, PLASTIC in 1 CARTON (36800-770-03) > 100 TABLET, COATED in 1 BOTTLE, PLASTIC2014-03-310000-00-00NoNoCurrent
36800-770-05368000770051 BOTTLE, PLASTIC in 1 CARTON (36800-770-05) > 225 TABLET, COATED in 1 BOTTLE, PLASTIC2014-03-312022-09-30NoNoCurrent
36800-770-1236800077012400 TABLET, COATED in 1 BOTTLE, PLASTIC (36800-770-12) 2016-01-012022-03-31NoNoCurrent