Acetaminophen Tablets

Manufacturer
Elysium Pharmaceuticals Ltd. | Elysium Pharmaceuticals Limited
Effective date
2026-01-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
monthly-update
Hydrated at
2026-06-03 17:51:24

Label at a glance#

ProductAcetaminophen
Active ingredientACETAMINOPHEN
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Acetaminophen USP 500mg

OTC - PURPOSE SECTION

for further packing and labelling 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

WARNINGS SECTION

keep out of reach of children and for further packing

INACTIVE INGREDIENT SECTION

Hypromellose, Magnesium stearate, Microcrystalline Cellulose , Pregelatinized Starch, Polyethylene Glycol, Povidone , Stearic Acid powder,Titanium Dioxide, Talc,

DOSAGE & ADMINISTRATION SECTION

anti-inflamatory and for further packing 

INDICATIONS & USAGE SECTION

Anti Inflamatory

SPL UNCLASSIFIED SECTION

label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
14803-01314803-013-00

Ingredients#

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

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

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
47b321ba-b503-1c86-e063-6294a90a0ae4a6eab0be-74ae-4743-882e-fb9f3181b8732026-01-06WarningsExact identifier
spl id: 47b321ba-b503-1c86-e063-6294a90a0ae4
spl set id: a6eab0be-74ae-4743-882e-fb9f3181b873

Reported adverse events (FAERS/openFDA)#

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