Acetaminophen

Product NDC: 30142-561
Requested package NDC: 30142-561-71
11-digit product format: 301420561
Labeler code: 30142
Product ID: 30142-561_09822782-9e5e-4ae3-b9ed-9b70ec05be0c
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen
Dosage form: TABLET
Route: ORAL
Labeler: Kroger Company
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 1987-07-15
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
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	30142-561	30142-561-71	D	Discontinued by firm		2026-08-17

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…`

Additional Listing Data#

Finished product: Yes
Brand name base: Acetaminophen
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 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
198440	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
8fb19444-f0e0-4d26-81e8-6a4b835056d8	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
30142-561-62	Acetaminophen	24 in 1 BOTTLE	TABLET	24	7
30142-561-62	Acetaminophen	1 in 1 CARTON	TABLET	1	7
30142-561-71	Acetaminophen	1 in 1 CARTON	TABLET	1	7
30142-561-71	Acetaminophen	50 in 1 BOTTLE	TABLET	50	7
30142-561-76	Acetaminophen	1 in 1 CARTON	TABLET	1	7
30142-561-76	Acetaminophen	120 in 1 BOTTLE	TABLET	120	7
30142-561-78	Acetaminophen	1 in 1 CARTON	TABLET	1	7
30142-561-78	Acetaminophen	100 in 1 BOTTLE	TABLET	100	7
30142-561-82	Acetaminophen	100 in 1 BOTTLE	TABLET	100	7
30142-561-82	Acetaminophen	2 in 1 CARTON	TABLET	2	7
30142-561-85	Acetaminophen	1 in 1 CARTON	TABLET	1	7
30142-561-85	Acetaminophen	250 in 1 BOTTLE	TABLET	250	7
30142-561-90	Acetaminophen	500 in 1 BOTTLE	TABLET	500	7

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ACETAMINOPHEN	ACTIVE INGREDIENT	362O9ITL9D	ACETAMINOPHEN TABLET [KROGER COMPANY]	2
ACETAMINOPHEN	ACTIVE MOIETY	362O9ITL9D	ACETAMINOPHEN TABLET [KROGER COMPANY]	2
CARNAUBA WAX	INACTIVE INGREDIENT	R12CBM0EIZ	ACETAMINOPHEN TABLET [KROGER COMPANY]	2
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	ACETAMINOPHEN TABLET [KROGER COMPANY]	2
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	ACETAMINOPHEN TABLET [KROGER COMPANY]	2
POLYETHYLENE GLYCOLS	INACTIVE INGREDIENT	3WJQ0SDW1A	ACETAMINOPHEN TABLET [KROGER COMPANY]	2
POVIDONES	INACTIVE INGREDIENT	FZ989GH94E	ACETAMINOPHEN TABLET [KROGER COMPANY]	2
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	ACETAMINOPHEN TABLET [KROGER COMPANY]	2
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	ACETAMINOPHEN TABLET [KROGER COMPANY]	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
30142-561	ACETAMINOPHEN TABLET [KROGER COMPANY]	7	Current NDC, Legacy NDC, 13 package rows	20241114_8fb19444-f0e0-4d26-81e8-6a4b835056d8.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 1 of 85 · 1,689 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Childrens Pain plus Fever Relief	ACETAMINOPHEN	CVS PHARMACY	e4cbfb06-d826-4d08-95d6-60305c417625	2026-08-14	Warnings	Exact identifier application number: M013
Childrens Pain Relief	ACETAMINOPHEN	CVS Pharmacy,Inc.	3738d35c-1e83-40df-9292-c54e6b2c8353	2026-08-14	Warnings	Exact identifier application number: M013
CVS Childrens Pain plus Fever Relief	ACETAMINOPHEN	CVS PHARMACY	22a48a33-995b-481e-9e4e-1ad7ec346f44	2026-08-14	Warnings	Exact identifier application number: M013
Pain Relief	ACETAMINOPHEN	Topco Associates, LLC	8b9e90da-98e2-4d8d-bf6e-54b0a8f8d101	2026-08-12	Warnings	Exact identifier application number: M013
Aspirin 81mg	ASPIRIN	HARRIS TEETER	54e69d5a-55d7-4ebe-8494-0be93613f1e2	2026-08-12	Warnings	Exact identifier application number: M013
Chewable Aspirin	ASPIRIN	HARRIS TEETER	c6a28c83-60c9-3304-e053-2a95a90aa06c	2026-08-12	Warnings	Exact identifier application number: M013
ASPIRIN	ASPIRIN	HARRIS TEETER	93cbd3cb-1072-89e6-e053-2995a90a2f15	2026-08-12	Warnings	Exact identifier application number: M013
Adult Chewable Aspirin	ASPIRIN	HARRIS TEETER	c6a28617-1769-7a7d-e053-2995a90a1ea0	2026-08-12	Warnings	Exact identifier application number: M013
Gencare- Pain Relief Acetaminophen	ACETAMINOPHEN	Pioneer Life Sciences, LLC	2111c91b-2fd7-4ab3-946a-d4e0cf46399a	2026-08-12	Warnings	Exact identifier application number: M013
Pain Reliever Extra Strength	ACETAMINOPHEN	Salado Sales, Inc.	1dbd8480-5cb4-4577-9091-b2a2add4f1af	2026-08-12	Warnings	Exact identifier application number: M013
pain relief childrens	ACETAMINOPHEN	Rite Aid Corporation	29ecdd2d-aeaf-40a8-a347-011088009ea6	2026-08-11	Warnings	Exact identifier application number: M013
Fast Acting Pedia Crae	ACETAMINOPHEN	Randob Labs., Ltd.	e069060f-fbb2-4c7a-b872-00b3ab86d01b	2026-08-11	Warnings	Exact identifier application number: M013
ASPIRIN	ASPIRIN	Amazon.com Services LLC	c7cc0681-4c0b-4565-99df-d0168c8ba1ba	2026-08-10	Warnings	Exact identifier application number: M013
GenCare Headache Relief	ACETAMINOPHEN, ASPIRIN, CAFFEINE	Pioneer Life Sciences, LLC	ac8c4bdf-30c9-2b09-e053-2a95a90a9b67	2026-08-09	Warnings	Exact identifier application number: M013
Gencare-Aspirin Low Dose Pain reliever (NSAID)	ASPIRIN	Pioneer Life Sciences, LLC	24d4f46a-c7a5-4e94-804f-1e307d8e8cfc	2026-08-09	Warnings	Exact identifier application number: M013
Aspirin 81 mg	ASPIRIN	DOLGENCORP, LLC	b4064039-2345-4227-b83d-54dc13a838d3	2026-08-07	Warnings	Exact identifier application number: M013
berkley and jensen acetaminophen	ACETAMINOPHEN	BJWC	dee57d73-73ac-48bb-b1da-9971f1ff21c4	2026-08-07	Warnings	Exact identifier application number: M013
Aspirin	ASPIRIN	P & L Development, LLC	4cd74cec-a209-4e92-b853-fbe5c95f7678	2026-08-06	Warnings	Exact identifier application number: M013
Tension Headache Aspirin-Free	ACETAMINOPHEN, CAFFEINE	Rite Aid Corporation	093a7c26-f2b1-4416-b193-81133d247d2e	2026-08-06	Warnings	Exact identifier application number: M013
ACETAMINOPHEN	ACETAMINOPHEN	Kroger Company	bc17b2e5-4828-6a2e-e053-2995a90a8c63	2026-08-05	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	8fb19444-f0e0-4d26-81e8-6a4b835056d8	7
198440	acetaminophen 500 MG Oral Tablet	SCD	8fb19444-f0e0-4d26-81e8-6a4b835056d8	7
198440	APAP 500 MG Oral Tablet	SY	8fb19444-f0e0-4d26-81e8-6a4b835056d8	7

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
30142-561-71	30142056171	1 BOTTLE in 1 CARTON (30142-561-71) > 50 TABLET in 1 BOTTLE	1 bottle	1987-07-15	0000-00-00	No	No	Current