Acetaminophen Tablets USP 500 mg

Manufacturer: Rescuers Life sciences Limited
Effective date: 2020-07-20
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:22:42

Label at a glance#

ProductAcetaminophen

Active ingredientACETAMINOPHEN

Label structure1 sections

Label contents#

Full prescribing information#

Acetaminophen Tablets 500 mg

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

acetaminophen-500mg-100 ct-jpg

acetaminophen-500mg-200 ct-jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
198440	acetaminophen 500 MG Oral Tablet	PSN	1
198440	acetaminophen 500 MG Oral Tablet	SCD	1
198440	APAP 500 MG Oral Tablet	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79583-001-01	2022-01-28	C162847	48780-1	d6a99b39-ac24-a426-e053-dadaa90af4c2	Acetaminophen Tablets USP 500 mg
79583-001-02	2022-01-28	C162847	48780-1	d6a99b39-ac24-a426-e053-dadaa90af4c2	Acetaminophen Tablets USP 500 mg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79583-001-01	Acetaminophen	100 in 1 BOTTLE	TABLET	100		1
79583-001-02	Acetaminophen	200 in 1 BOTTLE	TABLET	200		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79583-001	ACETAMINOPHEN TABLET [RESCUERS LIFE SCIENCES LIMITED]	1	2 package rows	20200727_71bcfe9e-e9c8-4cf6-9e17-39fbdb8e3962.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 10 matching rows.

Acetaminophen
MICROCRYSTALLINE CELLULOSE
SODIUM LAURYL SULFATE
MAGNESIUM STEARATE
METHYLPARABEN SODIUM
STARCH, CORN
SODIUM STARCH GLYCOLATE TYPE A
CROSCARMELLOSE SODIUM
TALC
POVIDONE K30

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79583-001	79583-001-01, 79583-001-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
MICROCRYSTALLINE CELLULOSE	OP1R32D61U	IACT
SODIUM LAURYL SULFATE	368GB5141J	IACT
MAGNESIUM STEARATE	70097M6I30	IACT
ACETAMINOPHEN	362O9ITL9D	ACTIB
METHYLPARABEN SODIUM	CR6K9C2NHK	IACT
STARCH, CORN	O8232NY3SJ	IACT
SODIUM STARCH GLYCOLATE TYPE A	H8AV0SQX4D	IACT
CROSCARMELLOSE SODIUM	M28OL1HH48	IACT
TALC	7SEV7J4R1U	IACT
POVIDONE K30	U725QWY32X	IACT

Source Document#

Source XML

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 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a06a2c1f-bdc1-447a-99ee-1e6384c98576			71bcfe9e-e9c8-4cf6-9e17-39fbdb8e3962	2020-07-20		Exact identifier spl id: a06a2c1f-bdc1-447a-99ee-1e6384c98576 spl set id: 71bcfe9e-e9c8-4cf6-9e17-39fbdb8e3962

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.