Extra Strength Acetaminophen

Manufacturer: Walgreens Company | Hi-Tech Nutraceuticals, LLC | Hi-Techn Nutraceutical, LLC
Effective date: 2022-12-31
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-05-31 23:52:49

Label at a glance#

ProductExtra Strength Acetaminophen

Active ingredientACETAMINOPHEN

Label structure16 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Drug Facts

OTC - ASK DOCTOR SECTION

Ask a Doctor Drug Facts

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a Doc or Pharm Drug Facts

OTC - DO NOT USE SECTION

Do not Use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach

OTC - PREGNANCY OR BREAST FEEDING SECTION

Pregnant

OTC - PURPOSE SECTION

Purpose

OTC - QUESTIONS SECTION

Questions or Comments? Call

OTC - STOP USE SECTION

Stop Use

OTC - WHEN USING SECTION

Directions

WARNINGS SECTION

Warnings

STORAGE AND HANDLING SECTION

Other Information

INACTIVE INGREDIENT SECTION

Inactives

INDICATIONS & USAGE SECTION

Uses

DOSAGE & ADMINISTRATION SECTION

Uses:
■ temporarily relieves minor aches and pains due to:
■ the common cold ■ headache ■backache
■ minor pain of arthritis ■ toothache ■ muscular aches
■ premenstrual and menstrual cramps
■ temporarily reduces fever

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
198440	acetaminophen 500 MG Oral Tablet	PSN	4
198440	acetaminophen 500 MG Oral Tablet	SCD	4
198440	APAP 500 MG Oral Tablet	SY	4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
0363-6973-02	2024-01-30	C162847	48780-1	1030e365-638b-111a-e063-dadaa90a10e2	Walgreens 125-Count Extra Strength

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0363-6973-02	Extra Strength Acetaminophen	125 in 1 BOTTLE, PLASTIC	TABLET	125		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0363-6973	EXTRA STRENGTH ACETAMINOPHEN (ACETAMINOPHEN) TABLET [WALGREENS COMPANY]	4	Legacy NDC, 1 package rows	20230101_ac079b3f-f4e6-671b-e053-2995a90a65c5.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

Extra Strength Acetaminophen
Acetaminophen
SODIUM STARCH GLYCOLATE TYPE A POTATO
HYPROMELLOSE, UNSPECIFIED
MAGNESIUM STEARATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0363-6973	0363-6973-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SODIUM STARCH GLYCOLATE TYPE A POTATO	5856J3G2A2	IACT
HYPROMELLOSE, UNSPECIFIED	3NXW29V3WO	IACT
MAGNESIUM STEARATE	70097M6I30	IACT
ACETAMINOPHEN	362O9ITL9D	ACTIB

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
f11c9344-b728-4cb2-e053-2a95a90aa8a0			ac079b3f-f4e6-671b-e053-2995a90a65c5	2022-12-31	Warnings	Exact identifier spl id: f11c9344-b728-4cb2-e053-2a95a90aa8a0 spl set id: ac079b3f-f4e6-671b-e053-2995a90a65c5

Reported adverse events (FAERS/openFDA)#

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