PLUSPHARMA EXTRA STRENGTH PAIN RELIEVER,FEVER REDUCER 500 MG

Manufacturer
direct rx
Effective date
2023-07-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:28:27

Label at a glance#

ProductPLUSPHARMA EXTRA STRENGTH PAIN RELIEVER,FEVER REDUCER 500 MG
Active ingredientACETAMINOPHEN
Label structure5 sections

Label contents#

Full prescribing information#

SPL MEDGUIDE SECTION

PlusPHARMA

See New Warnings Information and Directions

Extra Strength

ACETAMINOPHEN 500 mg

PAIN RELIEVER FEVER REDUCER

CONTAINS NO ASPIRIN

Compare to the Active Ingredient in Extra Strength Tylenol®

This product is not manufactured or distributed by McNeil Consumer Healthcare, owner of the registered trademark Extra Strength Tylenol®

SPL PATIENT PACKAGE INSERT SECTION

If you have any questions or comments, or to report an adverse event, please contact (800) 795-9775.

INACTIVE INGREDIENT SECTION

Povidone, Pregelatinized Starch, Sodium Starch Glycolate, Stearic Acid.

OTHER SAFETY INFORMATION

Do not use if imprinted safety seal under cap is broken or missing
Store at room temperature

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

012012

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72189-120-50EA - Each72189-120a1af2517-eb47-4c01-a06f-380414a5090512020-08-06
51645-706-01EA - Each51645-7069d69e3fa-cc3b-4b62-a473-63c1e4b8d08912022-10-06
51645-706-10EA - Each51645-7061ecd9f01-bdc1-4496-908c-9774c760dfd912021-11-09

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72189-12072189-120-50
51645-706

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
074b3b67-9274-33dd-e063-6394a90af29daa6cc288-ad0d-92e2-e053-2995a90a9e162023-10-09Exact identifier
spl set id: aa6cc288-ad0d-92e2-e053-2995a90a9e16

Reported adverse events (FAERS/openFDA)#

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