Pain Reliever

Product NDC: 68016-734
11-digit product format: 680160734
Labeler code: 68016
Product ID: 68016-734_24340ca1-73a1-ad18-e063-6394a90ab57c
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen
Dosage form: TABLET, COATED
Route: ORAL
Labeler: CHAIN DRUG CONSORTIUM
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2021-03-29
Marketing end: 2026-11-30
Substance: ACETAMINOPHEN
Active strength: 500 mg/1
NDC exclude flag: No
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	68016-734	68016-734-22	D	Discontinued by firm		2026-10-16
excluded package	package	68016-734	68016-734-50	D	Discontinued by firm		2026-10-16

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: Pain Reliever

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
5c1a3081-ae25-4895-bf76-ebcbb9fc8072	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
68016-734-01	Pain Reliever	100 in 1 BOTTLE, PLASTIC	TABLET, COATED	100	5
68016-734-01	Pain Reliever	1 in 1 CARTON	TABLET, COATED	1	5
68016-734-22	Pain Reliever	225 in 1 BOTTLE, PLASTIC	TABLET, COATED	225	5
68016-734-50	Pain Reliever	50 in 1 BOTTLE, PLASTIC	TABLET, COATED	50	5
68016-734-50	Pain Reliever	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
68016-734	PAIN RELIEVER (ACETAMINOPHEN) TABLET, COATED [CHAIN DRUG CONSORTIUM]	5	Current NDC, Legacy NDC, 5 package rows	20241013_5c1a3081-ae25-4895-bf76-ebcbb9fc8072.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 63 of 79 · 1,579 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
good sense childrens pain and fever	ACETAMINOPHEN	L. Perrigo Company	61a88a72-cf4f-4ec9-bc24-e110adfb98ba	2024-09-19	Warnings	Exact identifier application number: M013
childrens pain and fever	ACETAMINOPHEN	Walgreen Company	550c4229-c3a3-442c-a9ed-2d04cd4bad51	2024-09-14	Warnings	Exact identifier application number: M013
Rugby Aspirin	ASPIRIN	Rugby Laboratories	15922349-2825-45d3-95ff-c5a2879ec225	2024-09-12	Warnings	Exact identifier application number: M013
rexall pain relief	ACETAMINOPHEN	Dolgencorp, LLC	9783cf37-3a2b-4ca1-b4eb-6d6ba047a325	2024-09-12	Warnings	Exact identifier application number: M013
leader aspirin	ASPIRIN	Cardinal Health 110, LLC. dba Leader	b8cc9f78-a292-40eb-819d-bd80a552628f	2024-09-11	Warnings	Exact identifier application number: M013
pain relief	ACETAMINOPHEN	H E B	3258ef39-c36e-4a97-8631-89b8d4caf058	2024-09-11	Warnings	Exact identifier application number: M013
Acetaminophen and Diphenhydramine hydrochloride	ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE	KROGER COMPANY	b9b86755-63ad-e25a-e053-2995a90ad747	2024-09-10	Warnings	Exact identifier application number: M013
aspirin	ASPIRIN	Publix Super Markets Inc	88b0d897-b93f-42c3-88d0-784dd6c555e4	2024-09-10	Warnings	Exact identifier application number: M013
good neighbor pharmacy aspirin	ASPIRIN	Amerisource Bergen	820ceaee-2b49-4204-8ebb-d683d9b62e14	2024-09-10	Warnings	Exact identifier application number: M013
Parents Choice Infants Pain and Fever	ACETAMINOPHEN	Wal-Mart Stores Inc	30a51b90-a565-4e38-82ee-b5af29762977	2024-09-10	Warnings	Exact identifier application number: M013
equate aspirin chewable	ASPIRIN	Wal-Mart Stores Inc	9147c0ce-fcdb-457c-b9f5-e4edd66e91d0	2024-09-10	Warnings	Exact identifier application number: M013
signature care infants pain relief	ACETAMINOPHEN	Safeway	236df05a-cf11-42f3-a347-b54f5113680c	2024-09-10	Warnings	Exact identifier application number: M013
pain relief	ACETAMINOPHEN	Meijer Distribution Inc	d2759fa6-59cd-417e-8761-d2b129aad8b8	2024-09-09	Warnings	Exact identifier application number: M013
M-PAP	ACETAMINOPHEN	Bryant Ranch Prepack	d344479b-80c1-4592-acc8-3f12690c839c	2024-09-06	Warnings	Exact identifier application number: M013
signature care childrens pain relief	ACETAMINOPHEN	Safeway	fccb5aca-5707-491f-beb4-08f568919169	2024-09-06	Warnings	Exact identifier application number: M013
HEADACHE RELIEF	ACETAMINOPHEN-ASPIRIN-CAFFEINE	TARGET CORPORATION	8e953cef-135e-f1aa-e053-2995a90aaa8b	2024-09-05	Warnings	Exact identifier application number: M013
Aspirin	ASPIRIN	CVS Pharmacy	5cf74d72-c818-400a-9279-87e209efeb15	2024-09-05	Warnings	Exact identifier application number: M013
ASPIRN	ASPIRIN	HF Acquisition Co LLC, DBA HealthFirst	21524b42-f8fd-673c-e063-6294a90a22e8	2024-09-04	Warnings	Exact identifier application number: M013
Topcare Aspirin	ASPIRIN	Topco Associates LLC	6615bf85-1f79-4d21-91f9-4248c3cf9b38	2024-09-04	Warnings	Exact identifier application number: M013
ACETAMINOPHEN	ACETAMINOPHEN	TARGET CORPORATION	80da2582-1a20-e111-e053-2991aa0acf32	2024-09-03	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	5c1a3081-ae25-4895-bf76-ebcbb9fc8072	5
198440	acetaminophen 500 MG Oral Tablet	SCD	5c1a3081-ae25-4895-bf76-ebcbb9fc8072	5
198440	APAP 500 MG Oral Tablet	SY	5c1a3081-ae25-4895-bf76-ebcbb9fc8072	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
68016-734-01	68016073401	1 BOTTLE, PLASTIC in 1 CARTON (68016-734-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC	2021-03-29	2026-11-30	No	No	Current
68016-734-22	68016073422	225 TABLET, COATED in 1 BOTTLE, PLASTIC (68016-734-22)	2021-03-29	0000-00-00	No	No	Current
68016-734-50	68016073450	1 BOTTLE, PLASTIC in 1 CARTON (68016-734-50) > 50 TABLET, COATED in 1 BOTTLE, PLASTIC	2021-03-29	0000-00-00	No	No	Current