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 25 of 83 · 1,657 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Pain Reliever Extra Strength	ACETAMINOPHEN	L.N.K. International, Inc.	8fed703a-9de2-4c76-a783-fcf004f9b890	2026-01-07	Warnings	Exact identifier application number: M013
Aspirin	ASPIRIN	Amerisource Bergen	c3099892-a8cd-4574-a6f9-041e59e2feae	2026-01-07	Warnings	Exact identifier application number: M013
Bactimicina Childrens Pain and Fever	ACETAMINOPHEN	DLC Laboratories, Inc.	bdade270-d813-4178-b594-4951632b6839	2026-01-07	Warnings	Exact identifier application number: M013
Goodmeds Extra Strength Pain Relief PM	ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE	Cabinet Health P.B.C.	02c60967-46d7-49b7-82be-bc3c5fd36484	2026-01-06	Warnings	Exact identifier application number: M013
Childrens Acetaminophen	ACETAMINOPHEN	ARMY AND AIR FORCE EXCHANGE SERVICE	a73f8217-9eae-4e2a-b29c-7de3861d0e37	2026-01-06	Warnings	Exact identifier application number: M013
Pain Relief Acetaminophen PM	ACETAMINOPHEN AND DIPHENHYDRAMINE HCL	Rite Aid Corporation	f77f0120-4042-4b11-ba9c-cd35e1cd0bee	2026-01-05	Warnings	Exact identifier application number: M013
Menstrual Relief Maximum Strength	ACETAMINOPHEN, CAFFEINE AND PYRILAMINE MALEATE	United Natural Foods, Inc. dba UNFI	807598ef-9f03-48df-b076-3ee95ef4b06c	2026-01-05	Warnings	Exact identifier application number: M013
Pain Relief Extra Strength, Non-Aspirin	ACETAMINOPHEN	CHAIN DRUG MARKETING ASSOCIATION INC	1fb5e871-45fd-46fe-bf73-5192f8316e8e	2026-01-02	Warnings	Exact identifier application number: M013
Pain Reliever Extra Strength	ACETAMINOPHEN	Valu Merchandisers Company	0005aafa-08f8-4990-a54d-cc097195708f	2026-01-02	Warnings	Exact identifier application number: M013
Extra Strength Pain Reliever	ACETAMINOPHEN	Walmart Inc.	152bb455-da5b-ae13-e063-6394a90acab0	2026-01-01	Warnings	Exact identifier application number: M013
Dr. Cocoa for Children Pain and Fever	ACETAMINOPHEN	Infirst Healthcare Inc.	486ea294-6d18-a907-e063-6294a90ad284	2026-01-01	Warnings	Exact identifier application number: M013
ED APAP	ACETAMINOPHEN	EDWARDS PHARMACEUTICALS, INC.	f76d5fff-ebea-40f9-aad3-4064a0c863f0	2025-12-31	Warnings	Exact identifier application number: M013
EXTRA STRENGTH PAIN RELIEF	ACETAMINOPHEN	GERI-CARE PHARMACEUTICAL CORP	99ec63ef-aa28-c2fb-e053-2a95a90a9f6d	2025-12-31	Warnings	Exact identifier application number: M013
Puregen Labs Acetaminophen	ACETAMINOPHEN	Advanced Rx LLC	474580af-f6b0-e440-e063-6394a90aaada	2025-12-31	Warnings	Exact identifier application number: M013
Liquid Acetaminophen	ACETAMINOPHEN	LLORENS PHARMACEUTICALS INTERNATIONAL DIVISION	a7dbd4c0-53eb-4368-917b-1432c09ce6b4	2025-12-31	Warnings	Exact identifier application number: M013
Llorens Care Children Acetaminophen	ACETAMINOPHEN	Llorens Pharmaceutical International Division, Inc.	2a46d7d2-293b-5024-e063-6294a90a31aa	2025-12-31	Warnings	Exact identifier application number: M013
Pain Reliever	ACETAMINOPHEN CAPSULES 500MG (MINIS-RED OPAQUE)	Walgreens	3a801457-c5d0-b134-e063-6294a90ac5cb	2025-12-31	Warnings	Exact identifier application number: M013
Daytime and Nighttime Severe Cold and Flu combo pack	ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE	Genexa Inc.	190c7eaf-dcd4-d314-e063-6294a90a6f33	2025-12-30	Warnings	Exact identifier application number: M013
BioElectro Extra Strength Headache Relief	ACETAMINOPHEN, ASPIRIN, AND CAFFEINE	Genomma Lab USA	683a0fba-921c-48e7-a391-180c04f0d1c4	2025-12-30	Warnings	Exact identifier application number: M013
Pain Relief PM	ACETAMINOPHEN, DIPHENHYDRAMINE	Pioneer Life Sciences, LLC	0181af13-da32-4431-be39-c31fdfac9202	2025-12-29	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