Acetaminophen PM

Product NDC: 72036-171
11-digit product format: 720360171
Labeler code: 72036
Product ID: 72036-171_5852be42-2951-eb62-e063-6394a90afdc4
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen and Diphenhydramine Hydrochloride
Dosage form: TABLET, COATED
Route: ORAL
Labeler: Harris Teeter
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2014-06-06
Substance: ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Active strength: 500; 25 mg/1; mg/1
Pharmacologic classes: Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag: No
Listing certified through: 2027-12-31
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
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	72036-171	72036-171-03	D	Discontinued by firm		2026-10-15

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 · 12 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`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: Acetaminophen PM
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
ACETAMINOPHEN	500 mg/1
DIPHENHYDRAMINE HYDROCHLORIDE	25 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
362O9ITL9D	Internal UNII lookup
TC2D6JAD40	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
1092189	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
8a3e3439-90ae-4fc9-8ff2-44b8363fa338	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
0e2e0f88-b076-afe1-4bdd-32bca4375bec	Product name	3	20250127
3e48c9c4-918d-5d23-2f0b-d2398b06be54	Product name	1	20140508
865c72dd-0d94-daac-f728-ddd4ded2a79e	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
72036-171-02	Acetaminophen PM	40 in 1 BOTTLE, PLASTIC	TABLET, COATED	40	5
72036-171-02	Acetaminophen PM	1 in 1 CARTON	TABLET, COATED	1	5
72036-171-03	Acetaminophen PM	80 in 1 BOTTLE, PLASTIC	TABLET, COATED	80	5
72036-171-03	Acetaminophen PM	1 in 1 CARTON	TABLET, COATED	1	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72036-171	ACETAMINOPHEN PM (ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, COATED [HARRIS TEETER]	5	Current NDC, Legacy NDC, 4 package rows	20241024_8a3e3439-90ae-4fc9-8ff2-44b8363fa338.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 14 of 79 · 1,579 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Pain Reliever	ACETAMINOPHEN	HHH Pharmaceuticals	0c66b05d-132d-4c79-abfe-415fd68bbb9c	2026-05-06	Warnings	Exact identifier application number: M013
Aspirin	ASPIRIN	Better Living Brands, LLC	5ebd04d8-52c7-4c72-a4c1-fc7fd488ea24	2026-05-06	Warnings	Exact identifier application number: M013
Back and Body Extra Strength	ASPIRIN, CAFFEINE	Cardinal Health 110, LLC. DBA Leader	519eb216-9fa6-4d60-a2a4-3310bdb5b4ab	2026-05-06	Warnings	Exact identifier application number: M013
Aspirin	ASPIRIN	Geiss, Destin & Dunn Inc.	b8f6e486-5332-4c46-ab6c-7de04c91c60b	2026-05-06	Warnings	Exact identifier application number: M013
MAX relief junior Grape	CHILDRENS ACETAMINOPHEN	ATLANTIC BIOLOGICALS CORP.	c60494f0-5a50-41da-bcb4-88178ded54b7	2026-05-05	Warnings	Exact identifier application number: M013
equate pain relief pm	ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE	WALMART INC.	85129749-c1a7-4c4a-933f-c3c4768e2cdd	2026-05-05	Warnings	Exact identifier application number: M013
Acetaminophen Extra Strength	ACETAMINOPHEN	ARMY AND AIR FORCE EXCHANGE SERVICE	f3feca65-adc1-469f-bef6-12c860599abe	2026-05-04	Warnings	Exact identifier application number: M013
Childrens Pain and Fever	ACETAMINOPHEN	Strategic Sourcing Services LLC	4dda3534-4e83-447b-be75-33dadce06c47	2026-05-04	Warnings	Exact identifier application number: M013
Aspirin Low Dose Chewable Orange	ASPIRIN	Major Pharmaceuticals	4ba6eed3-004a-4576-b7f7-685fae49cf6a	2026-05-04	Warnings	Exact identifier application number: M013
Back and Body	ASPIRIN, CAFFEINE	Kroger Company	366b58db-1ac3-427b-b42a-5f56a14e298c	2026-05-01	Warnings	Exact identifier application number: M013
Tylenol PM	ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE	Savings Distributors LLC	8ed9a9f0-d37e-5c10-e053-2a95a90a559f	2026-05-01	Warnings	Exact identifier application number: M013
Tylenol Extra Strength	ACETAMINOPHEN	Savings Distributors LLC	8ed90757-833e-f4d9-e053-2995a90a29db	2026-05-01	Warnings	Exact identifier application number: M013
Acetaminophen , Aspirin and Caffeine	ACETAMINOPHEN , ASPIRIN AND CAFFEINE	Softgel Healthcare Pvt Ltd	4543e156-1deb-666e-e063-6394a90a719c	2026-04-27	Warnings	Exact identifier application number: M013
Acetaminophen , Caffeine and pyrilamine maleate	ACETAMINOPHEN , CAFFEINE AND PYRILAMINE MALEATE	Softgel Healthcare Pvt Ltd	45478958-ad86-4d87-e063-6394a90a3c45	2026-04-27	Warnings	Exact identifier application number: M013
Medique at Home Aspirin	ASPIRIN	Sportpharm LLC	0f2aa75e-534f-478b-811e-fb492b7af9bb	2026-04-24	Warnings	Exact identifier application number: M013
Medique at Home APAP Extra Strength	ACETAMINOPHEN 500 MG	Sportpharm LLC	cc280926-ad94-4017-a04a-b4315807eacb	2026-04-24	Warnings	Exact identifier application number: M013
Aspirin	ASPIRIN	Health Pharma USA LLC	503868bb-48e0-b718-e063-6394a90a9c5b	2026-04-24	Warnings	Exact identifier application number: M013
BC CHERRY	ASPIRIN AND CAFFEINE	Medtech Products Inc.	c5fa6660-a549-49ff-ac2b-5799afa22ec5	2026-04-24	Warnings	Exact identifier application number: M013
Doans Maximum Strength	MAGNESIUM SALICYLATE	Dr. Reddy's Laboratories Inc.	c906df41-bb45-03ea-b1a8-2b9816d55c97	2026-04-24	Warnings	Exact identifier application number: M013
Extra Strength Acetaminophen	ACETAMINOPHEN	TIME CAP LABORATORIES, INC.	48912649-9fa1-a11f-e063-6294a90a8a72	2026-04-23	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
TC2D6JAD40	DIPHENHYDRAMINE HYDROCHLORIDE	147-24-0	DIPHENHYDRAMINE HYDROCHLORIDE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1092189	acetaminophen 500 MG / diphenhydrAMINE HCl 25 MG Oral Tablet	PSN	8a3e3439-90ae-4fc9-8ff2-44b8363fa338	5
1092189	acetaminophen 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet	SCD	8a3e3439-90ae-4fc9-8ff2-44b8363fa338	5
1092189	APAP 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet	SY	8a3e3439-90ae-4fc9-8ff2-44b8363fa338	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
72036-171-02	72036017102	1 BOTTLE, PLASTIC in 1 CARTON (72036-171-02) / 40 TABLET, COATED in 1 BOTTLE, PLASTIC	2014-06-06	0000-00-00	No	No	Current
72036-171-03	72036017103	1 BOTTLE, PLASTIC in 1 CARTON (72036-171-03) > 80 TABLET, COATED in 1 BOTTLE, PLASTIC	2014-06-06	0000-00-00	No	No	Current