Tylenol Extra Strength

Product NDC: 67751-167
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	67751-167	67751-167-04	D	Discontinued by firm		2026-10-05
excluded package	package	67751-167	67751-167-03	D	Discontinued by firm		2026-10-05

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 · 30 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	67751-167-03	`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	67751-167-02	`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	67751-167-04	`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	67751-167-01	`1332a3947898…`	`d4bfe170f9cd…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded product	product		`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	67751-167-01	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	67751-167-04	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	67751-167-03	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-08-30 03:57 UTC · source 2022-08-29	excluded package	package	67751-167-02	`fb8cb913e6d1…`	`eb8c232b6be0…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded product	product		`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	67751-167-01	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	67751-167-04	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	67751-167-03	`86f5da6cb304…`	`a595104c45d7…`
2022-04-09 23:13 UTC · source 2022-04-08	excluded package	package	67751-167-02	`86f5da6cb304…`	`a595104c45d7…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded product	product		`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	67751-167-01	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	67751-167-04	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	67751-167-03	`bd6a592717d7…`	`303034d00443…`
2022-04-04 05:40 UTC · source 2022-04-01	excluded package	package	67751-167-02	`bd6a592717d7…`	`303034d00443…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded product	product		`8dfbde2a14a4…`	`c9ff85d89658…`
2021-12-27 23:28 UTC · source 2021-12-27	excluded package	package	67751-167-03	`8dfbde2a14a4…`	`c9ff85d89658…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded product	product		`e2bbac7714bc…`	`27bdfed8d636…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded package	package	67751-167-03	`e2bbac7714bc…`	`27bdfed8d636…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded product	product		`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	67751-167-03	`9bebd1f3094a…`	`5416666fcb17…`

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
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 · 2 matching rows.

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

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
86b6ac01-3866-4cd8-a1be-9babb6ff311b	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Indexing SPL table
NDC	Effective	Indexing SPL	Related label
67751-167-01	2024-04-17	d6a99b39-4b62-a426-e053-dadaa90af4c2	Tylenol Extra Strength
67751-167-02	2024-04-17	d6a99b39-4b62-a426-e053-dadaa90af4c2	Tylenol Extra Strength
67751-167-03	2024-04-17	9d75b9cf-e68d-f424-e053-dadaa90a57ce	Tylenol Extra Strength
67751-167-04	2024-04-17	d6a99b39-4b62-a426-e053-dadaa90af4c2	Tylenol Extra Strength
67751-167-01	2022-01-28	d6a99b39-4b62-a426-e053-dadaa90af4c2	Tylenol Extra Strength
67751-167-02	2022-01-28	d6a99b39-4b62-a426-e053-dadaa90af4c2	Tylenol Extra Strength
67751-167-04	2022-01-28	d6a99b39-4b62-a426-e053-dadaa90af4c2	Tylenol Extra Strength
67751-167-03	2020-01-31	9d75b9cf-e68d-f424-e053-dadaa90a57ce	Tylenol Extra Strength

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
67751-167-01	Tylenol Extra Strength	1 in 1 CARTON	TABLET, FILM COATED	1	6
67751-167-01	Tylenol Extra Strength	2 in 1 POUCH	TABLET, FILM COATED	2	6
67751-167-02	Tylenol Extra Strength	4 in 1 POUCH	TABLET, FILM COATED	4	6
67751-167-02	Tylenol Extra Strength	1 in 1 CARTON	TABLET, FILM COATED	1	6
67751-167-04	Tylenol Extra Strength	12 in 1 TRAY	TABLET, FILM COATED	12	6
67751-167-04	Tylenol Extra Strength	1 in 1 POUCH	TABLET, FILM COATED	1	6
67751-167-03	Tylenol Extra Strength	12 in 1 TRAY	TABLET, FILM COATED	12	2
67751-167-03	Tylenol Extra Strength	2 in 1 POUCH	TABLET, FILM COATED	2	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
67751-167	TYLENOL EXTRA STRENGTH (ACETAMINOPHEN) TABLET, FILM COATED [NAVAJO MANUFACTURING COMPANY INC.]	6	Current NDC, Legacy NDC, 6 package rows	20241004_86b6ac01-3866-4cd8-a1be-9babb6ff311b.zip
67751-167	TYLENOL EXTRA STRENGTH (ACETAMINOPHEN) TABLET, FILM COATED [NAVAJO MANUFACTURING COMPANY INC.]	2	Current NDC, Legacy NDC, 2 package rows	20240418_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 46 of 83 · 1,657 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Acetaminophen and Diphenhydramine Hydrochloride	ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE	Bi-Mart	70084eea-1480-4c46-b849-4c779319cb74	2025-07-02	Warnings	Exact identifier application number: M013
Acetaminophen, Aspirin, and Caffeine	ACETAMINOPHEN, ASPIRIN, AND CAFFEINE	Bi-Mart	40cd1a7a-e941-4503-8fe4-e939bd0d9d72	2025-07-02	Warnings	Exact identifier application number: M013
Maximum Strength Cough and Chest Congestion and Nighttime Severe Cold and Flu Combo pack	DEXTROMETHORPHAN HBR, GUAIFENESIN, ACETAMINOPHEN, DOXYLAMINE SUCCINATE	Genexa Inc.	18835205-a9e3-15c2-e063-6394a90a8107	2025-07-02	Warnings	Exact identifier application number: M013
FeverAll	ACETAMINOPHEN	Sun Pharmaceutical Industries, Inc.	8970b91b-5f3c-4764-9e23-25dcb398d0a7	2025-07-02	Warnings	Exact identifier application number: M013
Childrens Pain and Fever	ACETAMINOPHEN	Meijer Distribution Inc	11c9712d-c3b2-49cd-9c2b-0f57190c954e	2025-07-02	Warnings	Exact identifier application number: M013
Aspirin Regular Strength	ASPIRIN	United Natural Foods, Inc. dba UNFI	979973c1-661a-4384-8b92-fd901ebde558	2025-07-01	Warnings	Exact identifier application number: M013
Pain and Fever Childrens	ACETAMINOPHEN	CVS Pharmacy	f6bbce1c-9790-4ca4-847f-579c594ffe0b	2025-07-01	Warnings	Exact identifier application number: M013
Pain Reliever	ACETAMINOPHEN	WALGREENS	07d2e322-2465-79e5-e063-6294a90a5ea4	2025-06-30	Warnings	Exact identifier application number: M013
Pain Relief	ACETAMINOPHEN	DISCOUNT DRUG MART	66c0cf26-357b-4722-9100-3b86d507a8cd	2025-06-30	Warnings	Exact identifier application number: M013
ALLERGY	DIPHENHYDRAMINE HYDROCHLORIDE	Kroger Company	bc019c9e-8fac-5fd3-e053-2a95a90a7ccd	2025-06-25	Warnings	Exact identifier application number: M013
ACETAMINOPHEN Extra Strength	ACETAMINOPHEN	TIME CAP LABS INC	fd24d0e0-4f36-42d3-9149-2fb957690305	2025-06-25	Warnings	Exact identifier application number: M013
Aspirin Low Dose	ASPIRIN	ATLANTIC BIOLOGICALS CORP.	024c5054-959f-4ea5-a71f-c0e16cc4b90c	2025-06-24	Warnings	Exact identifier application number: M013
CHILDRENS ACETAMINOPHEN	CHILDRENS ACETAMINOPHEN ORAL	AARNA USA INC.	38070d15-2678-4e59-e063-6294a90ab690	2025-06-20	Warnings	Exact identifier application number: M013
TYLENOL Extra Strength	ACETAMINOPHEN	Morning Star OTC	8502ea21-937d-4b33-a3e0-ffab5dc38cd8	2025-06-19	Warnings	Exact identifier application number: M013
Tylenol PM Extra Strength	ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE	Morning Star OTC	6cd07a01-7034-4994-bbd3-bedcdf7d5b83	2025-06-19	Warnings	Exact identifier application number: M013
DRX CHOICE Tension Headache	ACETAMINOPHEN, CAFFEINE	Raritan Pharmaceuticals Inc.	8a5cb38b-669d-4177-b33b-d73c7ef48d18	2025-06-13	Warnings	Exact identifier application number: M013
good sense childrens pain and fever	ACETAMINOPHEN	NuCare Pharmaceuticals,Inc.	3777f4fb-d279-199d-e063-6394a90acf36	2025-06-13	Warnings	Exact identifier application number: M013
Aspirina Cafeina	ASPIRIN,CAFFEINE	Bayer HealthCare LLC.	2e709acc-325a-baca-e063-6394a90a24be	2025-06-12	Warnings	Exact identifier application number: M013
Aspirin	ASPIRIN	CHAIN DRUG MARKETING ASSOCIATION, INC.	696f55b1-536c-40c4-91f7-b572c39220db	2025-06-11	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	CVS Pharmacy, Inc.	6dea9e11-ff99-63c7-e053-2a91aa0a5b54	2025-06-10	Warnings	Exact identifier application number: M013

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
362O9ITL9D	ACETAMINOPHEN	103-90-2	ACETAMINOPHEN

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
198440	acetaminophen 500 MG Oral Tablet	PSN	86b6ac01-3866-4cd8-a1be-9babb6ff311b	6
209459	Tylenol Extra Strength 500 MG Oral Tablet	PSN	86b6ac01-3866-4cd8-a1be-9babb6ff311b	6
209459	acetaminophen 500 MG Oral Tablet [Tylenol]	SBD	86b6ac01-3866-4cd8-a1be-9babb6ff311b	6
198440	acetaminophen 500 MG Oral Tablet	SCD	86b6ac01-3866-4cd8-a1be-9babb6ff311b	6
198440	APAP 500 MG Oral Tablet	SY	86b6ac01-3866-4cd8-a1be-9babb6ff311b	6
209459	APAP 500 MG Oral Tablet [Tylenol]	SY	86b6ac01-3866-4cd8-a1be-9babb6ff311b	6
209459	Tylenol 500 MG Oral Tablet	SY	86b6ac01-3866-4cd8-a1be-9babb6ff311b	6
209459	Tylenol Extra Strength 500 MG Oral Tablet	SY	86b6ac01-3866-4cd8-a1be-9babb6ff311b	6
198440	acetaminophen 500 MG Oral Tablet	PSN	65bf1556-f25a-9439-e053-2a91aa0a3194	2
209459	Tylenol Extra Strength 500 MG Oral Tablet	PSN	65bf1556-f25a-9439-e053-2a91aa0a3194	2
209459	acetaminophen 500 MG Oral Tablet [Tylenol]	SBD	65bf1556-f25a-9439-e053-2a91aa0a3194	2
198440	acetaminophen 500 MG Oral Tablet	SCD	65bf1556-f25a-9439-e053-2a91aa0a3194	2
198440	APAP 500 MG Oral Tablet	SY	65bf1556-f25a-9439-e053-2a91aa0a3194	2
209459	APAP 500 MG Oral Tablet [Tylenol]	SY	65bf1556-f25a-9439-e053-2a91aa0a3194	2
209459	Tylenol 500 MG Oral Tablet	SY	65bf1556-f25a-9439-e053-2a91aa0a3194	2
209459	Tylenol Extra Strength 500 MG Oral Tablet	SY	65bf1556-f25a-9439-e053-2a91aa0a3194	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
67751-167-01	67751016701	1 POUCH in 1 CARTON (67751-167-01) / 2 TABLET, FILM COATED in 1 POUCH	1 pouch	2016-09-22	0000-00-00	No	No	Current
67751-167-02	67751016702	1 POUCH in 1 CARTON (67751-167-02) / 4 TABLET, FILM COATED in 1 POUCH	1 pouch	2016-09-22	0000-00-00	No	No	Current
67751-167-03	67751016703	12 in 1 TRAY						Historical
67751-167-04	67751016704	12 POUCH in 1 TRAY (67751-167-04) > 1 TABLET, FILM COATED in 1 POUCH	12 pouch	2016-09-22	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Tylenol Extra Strength	Navajo Manufacturing Company Inc.	2024-10-02	HUMAN OTC DRUG LABEL	6
Tylenol Extra Strength	Navajo Manufacturing Company Inc. \| Navajo Manufacutring Company Inc.	2024-04-15	HUMAN OTC DRUG LABEL	2