FDA.reportPublic FDA data

Tylenol Extra Strength

Product NDC
67751-167
Requested package NDC
67751-167-04
11-digit product format
677510167
Labeler code
67751
Product ID
67751-167_2385e645-881c-5dd8-e063-6394a90adfab
Type
HUMAN OTC DRUG
Nonproprietary name
ACETAMINOPHEN
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Navajo Manufacturing Company Inc.
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2016-09-22
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 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage67751-16767751-167-04DDiscontinued by firm2026-10-23

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 · 4 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2024-03-11 06:39 UTC · source 2024-03-081332a3947898…d4bfe170f9cd…
2022-08-30 03:57 UTC · source 2022-08-29fb8cb913e6d1…eb8c232b6be0…
2022-04-09 23:13 UTC · source 2022-04-0886f5da6cb304…a595104c45d7…
2022-04-04 05:40 UTC · source 2022-04-01bd6a592717d7…303034d00443…

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
Tylenol 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 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
198440Internal RxNorm lookup
209459Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
86b6ac01-3866-4cd8-a1be-9babb6ff311bAvailable on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Indexing SPL table
NDCEffectiveIndexing SPLRelated label
67751-167-012024-04-17d6a99b39-4b62-a426-e053-dadaa90af4c2Tylenol Extra Strength
67751-167-022024-04-17d6a99b39-4b62-a426-e053-dadaa90af4c2Tylenol Extra Strength
67751-167-032024-04-179d75b9cf-e68d-f424-e053-dadaa90a57ceTylenol Extra Strength
67751-167-042024-04-17d6a99b39-4b62-a426-e053-dadaa90af4c2Tylenol Extra Strength
67751-167-012022-01-28d6a99b39-4b62-a426-e053-dadaa90af4c2Tylenol Extra Strength
67751-167-022022-01-28d6a99b39-4b62-a426-e053-dadaa90af4c2Tylenol Extra Strength
67751-167-042022-01-28d6a99b39-4b62-a426-e053-dadaa90af4c2Tylenol Extra Strength
67751-167-032020-01-319d75b9cf-e68d-f424-e053-dadaa90a57ceTylenol Extra Strength

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67751-167-01Tylenol Extra Strength1 in 1 CARTONTABLET, FILM COATED16
67751-167-01Tylenol Extra Strength2 in 1 POUCHTABLET, FILM COATED26
67751-167-02Tylenol Extra Strength4 in 1 POUCHTABLET, FILM COATED46
67751-167-02Tylenol Extra Strength1 in 1 CARTONTABLET, FILM COATED16
67751-167-04Tylenol Extra Strength12 in 1 TRAYTABLET, FILM COATED126
67751-167-04Tylenol Extra Strength1 in 1 POUCHTABLET, FILM COATED16
67751-167-03Tylenol Extra Strength12 in 1 TRAYTABLET, FILM COATED122
67751-167-03Tylenol Extra Strength2 in 1 POUCHTABLET, FILM COATED22

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67751-167TYLENOL EXTRA STRENGTH (ACETAMINOPHEN) TABLET, FILM COATED [NAVAJO MANUFACTURING COMPANY INC.]6Current NDC, Legacy NDC, 6 package rows20241004_86b6ac01-3866-4cd8-a1be-9babb6ff311b.zip
67751-167TYLENOL EXTRA STRENGTH (ACETAMINOPHEN) TABLET, FILM COATED [NAVAJO MANUFACTURING COMPANY INC.]2Current NDC, Legacy NDC, 2 package rows20240418_65bf1556-f25a-9439-e053-2a91aa0a3194.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 76 of 79 · 1,570 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AcetaminophenACETAMINOPHENAurohealth LLC30756257-f748-4a5d-b031-dd267d0f91ad2023-11-29WarningsExact identifier
application number: M013
Aurophen Regular StrengthACETAMINOPHENAurohealth LLC8eda893f-5266-4b7a-95b9-2e194973cf062023-11-29WarningsExact identifier
application number: M013
Childrens Pain ReliefACETAMINOPHENAurohealth LLC00ec6518-b5e3-49d1-a342-139381c3bfd22023-11-29WarningsExact identifier
application number: M013
CHILDRENS PAIN RELIEFACETAMINOPHENBetter Living Brands, LLCfadb4c09-071f-56c0-e053-6294a90ae6c12023-11-28WarningsExact identifier
application number: M013
Acetaminophen and Diphenhydramine hydrochlorideACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDEBetter Living Brands, LLCfc07d516-9ffe-9989-e053-6294a90ae1a52023-11-28WarningsExact identifier
application number: M013
NOTTS - Tension HeadacheACETAMINOPHEN, CAFFEINEVIVUNT PHARMA LLC08f2ae03-967b-ad7e-e063-6294a90a84842023-11-24WarningsExact identifier
application number: M013
Sanatos Multi Symptoms NighttimeACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATEPharmadel LLC0a60326a-a17b-e843-e063-6394a90ac2112023-11-22WarningsExact identifier
application number: M013
Sanatos Nighttime Multi SymptomsACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATEPharmadel LLC0ab188f3-f7f9-d665-e063-6294a90a198a2023-11-22WarningsExact identifier
application number: M013
ASPIRINASPIRINTIME CAP LABS INCfe12519c-3e5f-4592-bd34-2d6b81b981f42023-11-22WarningsExact identifier
application number: M013
Rugby Regular Strength AcetaminophenACETAMINOPHENA-S Medication Solutions400d4a29-9e39-4e74-8272-37be5d7899242023-11-22WarningsExact identifier
application number: M013
RIGHT REMEDIES Pain Relief Extra Strength CapletACETAMINOPHENStrive Pharmaceuticals Inc.dcce28d9-8528-489e-b995-1d98e9d0e6ad2023-11-21WarningsExact identifier
application number: M013
Sanatos Multi Symptom DaytimeACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCIPharmadel LLC0ab11691-5b29-55fc-e063-6394a90aa3282023-11-17WarningsExact identifier
application number: M013
AcetaminophenACETAMINOPHENA-S Medication Solutions1e223faa-f6d0-4235-bc4c-6cfca84a5b0a2023-11-17WarningsExact identifier
application number: M013
SanaTos XACETAMINOPHEN, DEXTROMETHORPHAN HBR,GUAIFENESIN, PHENYLEPHRINE HCIPharmadel LLC85b8ef3d-7318-7f3b-e053-2991aa0a07772023-11-14WarningsExact identifier
application number: M013
RIGHT REMEDIES EXTRA STRENGTH PM Pain ReliefACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDEStrive Pharmaceuticals Inc.8badbaad-eb35-4251-a779-00474819360d2023-11-13WarningsExact identifier
application number: M013
AcetaminophenACETAMINOPHENTrifecta Pharmaceuticals USA LLC09935a74-34b0-0e7c-e063-6294a90a7c832023-11-07WarningsExact identifier
application number: M013
Pain Relief PMACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDEAMERIFOODS TRADING COMPANYf6dd6396-93e9-1096-e053-6394a90af06d2023-11-02WarningsExact identifier
application number: M013
AcetaminophenACETAMINOPHENRETAIL BUSINESS SERVICES , LLC.eb644e9e-36dc-5f84-e053-2a95a90affa52023-11-02WarningsExact identifier
application number: M013
Good Sense Childrens Pain and FeverACETAMINOPHENProficient Rx LP46527b1f-7515-44ce-b5cb-9d24223b9af12023-11-01WarningsExact identifier
application number: M013
AspirinASPIRINA-S Medication Solutions12feb32b-4b8c-4b17-9e86-cb286457b0882023-11-01WarningsExact identifier
application number: M013

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198440acetaminophen 500 MG Oral TabletPSN86b6ac01-3866-4cd8-a1be-9babb6ff311b6
209459Tylenol Extra Strength 500 MG Oral TabletPSN86b6ac01-3866-4cd8-a1be-9babb6ff311b6
209459acetaminophen 500 MG Oral Tablet [Tylenol]SBD86b6ac01-3866-4cd8-a1be-9babb6ff311b6
198440acetaminophen 500 MG Oral TabletSCD86b6ac01-3866-4cd8-a1be-9babb6ff311b6
198440APAP 500 MG Oral TabletSY86b6ac01-3866-4cd8-a1be-9babb6ff311b6
209459APAP 500 MG Oral Tablet [Tylenol]SY86b6ac01-3866-4cd8-a1be-9babb6ff311b6
209459Tylenol 500 MG Oral TabletSY86b6ac01-3866-4cd8-a1be-9babb6ff311b6
209459Tylenol Extra Strength 500 MG Oral TabletSY86b6ac01-3866-4cd8-a1be-9babb6ff311b6
198440acetaminophen 500 MG Oral TabletPSN65bf1556-f25a-9439-e053-2a91aa0a31942
209459Tylenol Extra Strength 500 MG Oral TabletPSN65bf1556-f25a-9439-e053-2a91aa0a31942
209459acetaminophen 500 MG Oral Tablet [Tylenol]SBD65bf1556-f25a-9439-e053-2a91aa0a31942
198440acetaminophen 500 MG Oral TabletSCD65bf1556-f25a-9439-e053-2a91aa0a31942
198440APAP 500 MG Oral TabletSY65bf1556-f25a-9439-e053-2a91aa0a31942
209459APAP 500 MG Oral Tablet [Tylenol]SY65bf1556-f25a-9439-e053-2a91aa0a31942
209459Tylenol 500 MG Oral TabletSY65bf1556-f25a-9439-e053-2a91aa0a31942
209459Tylenol Extra Strength 500 MG Oral TabletSY65bf1556-f25a-9439-e053-2a91aa0a31942

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
67751-167-046775101670412 POUCH in 1 TRAY (67751-167-04) > 1 TABLET, FILM COATED in 1 POUCH12 pouch2016-09-220000-00-00NoNoCurrent