pain relief

Product NDC: 56062-192
11-digit product format: 560620192
Labeler code: 56062
Product ID: 56062-192_2433b664-cded-f976-e063-6394a90a2975
Type: HUMAN OTC DRUG
Nonproprietary name: Acetaminophen
Dosage form: TABLET, COATED
Route: ORAL
Labeler: PUBLIX SUPER MARKETS INC
Application: M013
Marketing category: OTC MONOGRAPH DRUG
Marketing start: 2020-05-01
Marketing end: 2026-12-31
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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	56062-192	56062-192-03	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 relief

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
9e779cc6-4641-6132-e053-2a95a90a3493	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
56062-192-01	pain relief	100 in 1 BOTTLE, PLASTIC	TABLET, COATED	100	3
56062-192-01	pain relief	1 in 1 CARTON	TABLET, COATED	1	3
56062-192-03	pain relief	1 in 1 CARTON	TABLET, COATED	1	3
56062-192-03	pain relief	50 in 1 BOTTLE, PLASTIC	TABLET, COATED	50	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
56062-192	PAIN RELIEF (ACETAMINOPHEN) TABLET, COATED [PUBLIX SUPER MARKETS INC]	3	Current NDC, Legacy NDC, 4 package rows	20241013_9e779cc6-4641-6132-e053-2a95a90a3493.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 49 of 79 · 1,579 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Low dose Aspirin	ASPIRIN 81 MG DELAYED RELEASE TABLETS	WALGREENS	c25c3524-3e24-3410-e053-2995a90a73ed	2025-01-30	Warnings	Exact identifier application number: M013
HEADACHE RELIEF	ACETAMINOPHEN, ASPIRIN, CAFFEINE	WALGREENS	b5a45daa-05b1-4d6d-e053-2995a90a8444	2025-01-30	Warnings	Exact identifier application number: M013
Aspirin 81	ASPIRIN	WALGREENS	d71a571e-e2ce-7e0a-e053-2a95a90a53e0	2025-01-30	Warnings	Exact identifier application number: M013
Regular strength aspirin	ASPIRIN	TARGET CORPORATION	e8c87ccb-8c0c-7830-e053-2995a90a88b7	2025-01-30	Warnings	Exact identifier application number: M013
Multi-Symptom Menstrual Relief	ACETAMINOPHEN, CAFFEINE, PYRILAMINE MALEATE	TARGET	2368ac1b-d644-9908-e063-6394a90a4b89	2025-01-29	Warnings	Exact identifier application number: M013
Pain Reliever Extra Strength	ACETAMINOPHEN	Walgreen Company	28e275fb-d615-4725-998c-946fe1bfdc0c	2025-01-29	Warnings	Exact identifier application number: M013
Childrens Acetaminophen	ACETAMINOPHEN	Major Pharmaceuticals	38b839b6-de7d-4f33-a19a-efc92cdad92c	2025-01-24	Warnings	Exact identifier application number: M013
good sense pain relief	ACETAMINOPHEN	Preferred Pharmaceuticals Inc.	523b68da-cd2a-4960-95e7-de5d51ce33c1	2025-01-23	Warnings	Exact identifier application number: M013
Safety Coated Aspirin 81 mg Low Dose	ASPIRIN 81MG	Ulai Health LLC	3d225a11-a53b-4dc2-9c25-13cab007900f	2025-01-20	Warnings	Exact identifier application number: M013
Pharbetol	ACETAMINOPHEN 325 MG	Ulai Health LLC	55bb7e6c-e98c-48bd-b7bb-9848ff0273ca	2025-01-20	Warnings	Exact identifier application number: M013
ACETAMINOPHEN PM	ACETAMINOPHEN 500MG / DIPHENHYDRAMINE HCL 25MG	Ulai Health LLC	d4a568c9-a721-48d1-aebc-fc65444947ce	2025-01-20	Warnings	Exact identifier application number: M013
Pharbetol	ACETAMINOPHEN 500MG	Ulai Health LLC	c9d3cee1-531c-439f-ae19-07acd366aad6	2025-01-20	Warnings	Exact identifier application number: M013
Percogesic Original Strength	ACETAMINOPHEN AND DIPHENHYDRAMINE HCL	Medtech Products Inc.	529974c2-0121-4892-8e47-c2c447581091	2025-01-17	Warnings	Exact identifier application number: M013
Little Remedies Childrens Fever Pain Reliever	ACETAMINOPHEN	Medtech Products Inc.	e1e44c85-d10c-4997-8f85-064cda7906eb	2025-01-17	Warnings	Exact identifier application number: M013
Stanback	ASPIRIN AND CAFFEINE	Medtech Products Inc.	caaa1313-09e4-45aa-8836-346f6a370196	2025-01-17	Warnings	Exact identifier application number: M013
Dye Free Childrens Acetaminophen	ACETAMINOPHEN	Precision Dose Inc.	5cc698fa-0841-4851-ae21-0aac8b40eb0a	2025-01-16	Warnings	Exact identifier application number: M013
Ecotrin	ASPIRIN	Medtech Products Inc.	222d187b-aae6-410b-baeb-b2bd42f5c676	2025-01-16	Warnings	Exact identifier application number: M013
Children Pain and Fever Reliever	ACETAMINOPHEN	Target Corporation	0dd643a4-3cbc-423d-95b4-ba373b09d895	2025-01-16	Warnings	Exact identifier application number: M013
Chewable Low Dose Aspirin	ASPIRIN	TARGET CORPORATION	f934e72a-2e9f-da17-e053-6394a90a1a2e	2025-01-15	Warnings	Exact identifier application number: M013
ACETAMINOPHEN 500 MG	ACETAMINOPHEN	Reliable 1 Laboratories LLC	2651bf11-4d66-43ba-e054-00144ff88e88	2025-01-15	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	9e779cc6-4641-6132-e053-2a95a90a3493	3
198440	acetaminophen 500 MG Oral Tablet	SCD	9e779cc6-4641-6132-e053-2a95a90a3493	3
198440	APAP 500 MG Oral Tablet	SY	9e779cc6-4641-6132-e053-2a95a90a3493	3

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
56062-192-01	56062019201	1 BOTTLE, PLASTIC in 1 CARTON (56062-192-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC	2020-05-01	2026-12-31	No	No	Current
56062-192-03	56062019203	1 BOTTLE, PLASTIC in 1 CARTON (56062-192-03) > 50 TABLET, COATED in 1 BOTTLE, PLASTIC	2020-05-01	0000-00-00	No	No	Current