Acetaminophen PM

Product NDC: 69842-956
11-digit product format: 698420956
Labeler code: 69842
Product ID: 69842-956_47ca6770-e94f-4ccf-ac53-ddbccfd93d22
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen, Diphenhydramine HCl
Dosage form: TABLET, COATED
Route: ORAL
Labeler: CVS PHARMACY
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2007-12-17
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	69842-956	69842-956-09	D	Discontinued by firm		2026-10-27
excluded package	package	69842-956	69842-956-13	D	Discontinued by firm		2026-10-27

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 · 24 matching rows.

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

Captured / source date, Package NDC, Snapshot table
Captured / source date	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	69842-956-13	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	69842-956-09	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	69842-956-13	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	69842-956-09	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	69842-956-13	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	69842-956-09	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	69842-956-13	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	69842-956-09	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	69842-956-13	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	69842-956-09	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	69842-956-13	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	69842-956-09	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	69842-956-13	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	69842-956-09	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	69842-956-13	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	69842-956-09	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	69842-956-13	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	69842-956-09	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	69842-956-13	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	69842-956-09	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	69842-956-13	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	69842-956-09	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	69842-956-09	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	69842-956-13	`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
Brand name suffix: Extra Strength
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
67a190c3-7de0-4f57-be94-d6b8285e1220	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
69842-956-09	Acetaminophen PMExtra Strength	1 in 1 CARTON	TABLET, COATED	1	12
69842-956-09	Acetaminophen PMExtra Strength	20 in 1 BOTTLE, PLASTIC	TABLET, COATED	20	12
69842-956-13	Acetaminophen PMExtra Strength	250 in 1 BOTTLE	TABLET, COATED	250	12
69842-956-31	Acetaminophen PMExtra Strength	80 in 1 BOTTLE, PLASTIC	TABLET, COATED	80	12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69842-956	ACETAMINOPHEN PM EXTRA STRENGTH (ACETAMINOPHEN, DIPHENHYDRAMINE HCL) TABLET, COATED [CVS PHARMACY]	11	Current NDC, Legacy NDC, 4 package rows	20250327_67a190c3-7de0-4f57-be94-d6b8285e1220.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 74 of 79 · 1,561 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Tension Headache Pain Relieving Aid	ACETAMINOPHEN,CAFFEINE	WAL-MART STORES INC	00fadd26-a6eb-dc5e-e063-6394a90a3cca	2023-12-15	Warnings	Exact identifier application number: M013
Dye-Free Aspirin 81	ASPIRIN	WALGREENS	d71a9d3a-cd28-14a8-e053-2995a90a832b	2023-12-15	Warnings	Exact identifier application number: M013
Lil Drug Store Aspirin 325	ASPIRIN	Lil Drug Store Products, Inc	de59aae2-f794-4243-acc8-37a10e27abde	2023-12-15	Warnings	Exact identifier application number: M013
Pain Reliever	ACETAMINOPHEN TABLET, EXTRA STRENGTH	Lil' Drug Store Products, Inc.	f0fdab5a-9d07-57aa-e053-2a95a90adc7f	2023-12-15	Warnings	Exact identifier application number: M013
BC Cherry	ASPIRIN AND CAFFEINE	Lil' Drug Store Products, Inc	79ea721b-d656-44f7-9d13-390debee7be0	2023-12-15	Warnings	Exact identifier application number: M013
Alka-Seltzer	BUFFERED ASPIRIN	Lil' Drug Store Products, Inc.	0c7a60e7-0bde-9aa2-e063-6294a90a3209	2023-12-14	Warnings	Exact identifier application number: M013
Circle K Aspirin 325	ASPIRIN	Lil Drug Store Products, Inc	4cd306e3-2119-4272-9da4-a848fe2746fa	2023-12-14	Warnings	Exact identifier application number: M013
Circle K Pain Reliever Extra Strength	ACETAMINOPHEN	Lil' Drug Store Products, Inc.	f2359bc3-901f-4ecb-b402-cb2fe404a935	2023-12-14	Warnings	Exact identifier application number: M013
Childrens Pain Relief	ACETAMINOPHEN	DISCOUNT DRUG MART	c55b8f9d-1396-43c0-acc9-5e3485eadb07	2023-12-08	Warnings	Exact identifier application number: M013
Childrens Pain Relief	ACETAMINOPHEN	DISCOUNT DRUG MART	775519ad-5683-451f-9bfc-5fafc70c68ec	2023-12-08	Warnings	Exact identifier application number: M013
Acetaminophen	ACETAMINOPHEN	WALGREEN CO.	c20c814b-35f5-4c46-e053-2a95a90a50f2	2023-12-08	Warnings	Exact identifier application number: M013
Acetaminophen Extra Strength	ACETAMINOPHEN	Better Living Brands LLC	f9859be4-6d0b-2ab8-e053-6294a90aa862	2023-12-06	Warnings	Exact identifier application number: M013
Aurophen Regular Strength	ACETAMINOPHEN	KROGER COMPANY	b9b7b849-c3b3-9af7-e053-2a95a90a0077	2023-12-06	Warnings	Exact identifier application number: M013
Acetaminophen Regular Strength	ACETAMINOPHEN	KROGER COMPANY	cf649478-57d2-cc88-e053-2a95a90ad1ba	2023-12-06	Warnings	Exact identifier application number: M013
Acetaminophen Extra Strength	ACETAMINOPHEN	KROGER COMPANY	b9b6f878-1ec8-3dc0-e053-2995a90a5414	2023-12-06	Warnings	Exact identifier application number: M013
Pain Reliever	ACETAMINOPHEN	WALGREEN CO.	a48c522c-76c5-49f8-8c4d-3ee6b221e6f3	2023-12-06	Warnings	Exact identifier application number: M013
Pain Reliever	ACETAMINOPHEN	WALGREEN CO.	cc939a7c-ce56-5dd6-e053-2995a90aa8af	2023-12-06	Warnings	Exact identifier application number: M013
Alka-Seltzer Original Flavor	BUFFERED ASPIRIN, EFFERVESCENT TABLET	Lil' Drug Store Products, Inc.	ea5df8be-a08c-5fa3-e053-2995a90a0bac	2023-12-06	Warnings	Exact identifier application number: M013
Ringl	ACETAMINOPHEN	Sato Pharmaceutical Co., Ltd.	ba5a0286-3e0f-4bef-96e5-29d92f51f432	2023-12-06	Warnings	Exact identifier application number: M013
Pain Relief Childrens	ACETAMINOPHEN	Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)	41633554-474e-4d3c-9187-d90487d2ae8c	2023-12-06	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	67a190c3-7de0-4f57-be94-d6b8285e1220	12
1092189	acetaminophen 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet	SCD	67a190c3-7de0-4f57-be94-d6b8285e1220	12
1092189	APAP 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet	SY	67a190c3-7de0-4f57-be94-d6b8285e1220	12

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
69842-956-09	69842095609	1 BOTTLE, PLASTIC in 1 CARTON (69842-956-09) > 20 TABLET in 1 BOTTLE, PLASTIC	2007-12-17	0000-00-00	No	No	Current
69842-956-13	69842095613	250 in 1 BOTTLE					Historical
69842-956-31	69842095631	80 TABLET, COATED in 1 BOTTLE, PLASTIC (69842-956-31)	2007-12-17	0000-00-00	No	No	Current