Nuvicare-Pain Relief Acetaminophen 325 mg Tablets

Manufacturer
NUVICARE LLC
Effective date
2026-08-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-08-06 06:10:30

Label at a glance#

ProductPain Relief Acetaminophen 325 mg
Active ingredientAcetaminophen
Label structure17 sections

Indications and uses

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

Dosage and administration

■ Do not take more than directed (see overdose warning)  adults and children 12 years and over  ■ take 2 tablets every 4 to 6 hours while symptoms last  ■ do not take more than 10 tablets in 24 hours, unless directed by a doctor  ■ do not use for more than 10 days unless directed by a doctor children 6 years to under 12 years  ■ take 1 tablet every 4 to 6 hours while symptoms last  ■ do not take more than 5 tablet...

Label contents#

Full prescribing information#

Active Ingredient (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Acetaminophen 325 mg

Purpose

OTC - PURPOSE SECTION

Pain reliever/fever reducer

Uses

INDICATIONS & USAGE SECTION

temporarily relieves minor aches and pains due to:

■ headache

■ muscular aches

■ backache

■ minor pain of arthritis

■ the common cold

■ toothache
■ premenstrual and menstrual cramps
■ temporarily reduces fever

Warnings

WARNINGS SECTION

Liver warning: This product contains acetaminophen. The maximum daily dose of this product is 10 tablets (3,250 mg) in 24 hours for adults or 5 tablets (1,625 mg) in 24 hours for children. Severe liver damage may occur if

■ adult takes more than 4,000 mg of acetaminophen in 24 hours

■ child takes more than 5 doses in 24 hours, which is the maximum daily amount

■ taken with other drugs containing acetaminophen

■ adult has 3 or more alcoholic drinks every day while using this product

Allergy alert: acetaminophen may cause severe skin reactions. Symptoms may include:

■ skin reddening

■ blisters

■ rash

If a skin reaction occurs, stop use and seek medical help right away.

OTC - DO NOT USE SECTION

Do not use

■ with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist. ■ if you are allergic to acetaminophen or any of the inactive ingredients in this product

OTC - ASK DOCTOR SECTION

Ask a doctor before use if the user has liver disease

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor or pharmacist before use if the user is taking the blood thinning drug warfarin

OTC - STOP USE SECTION

Stop use and ask a doctor if

■ pain gets worse or lasts more than 10 days in adults

■pain gets worse or lasts more than 5 days in children under 12 years
■ fever gets worse or lasts more than 3 days

■ new symptoms occur

■ redness or swelling is present
These could be signs of a serious condition.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OVERDOSAGE SECTION

Overdose warning: In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222) Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Do not take more than directed (see overdose warning)

 adults and children 12 years and over

 ■ take 2 tablets every 4 to 6 hours while symptoms last

 ■ do not take more than 10 tablets in 24 hours, unless directed by a doctor

 ■ do not use for more than 10 days unless directed by a doctor

children 6 years to under 12 years

 ■ take 1 tablet every 4 to 6 hours while symptoms last

 ■ do not take more than 5 tablets in 24 hours
 ■ do not use for more than 5 days unless directed by a doctor

children under 6 years ask a doctor

Other information

OTHER SAFETY INFORMATION

■ Store between 20° to 25°C (68° to 77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

hypromellose-5, hypromellose-15, magnesium stearate, microcrystalline cellulose, polyethylene glycol-400, polyvinyl pyrrolidone, pregelatinized starch, stearic acid powder, talc, titanium dioxide.

Questions or comments?

OTC - QUESTIONS SECTION

Call +1 (718) 337-8733 or email: support@nuvicare.com

SPL UNCLASSIFIED SECTION

†This product is neither manufactured nor distributed by Kenvue Brands LLC, owner of the registered trademark TYLENOL®.

NDC 84324-046-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

L188-00 NC-Pain Relief-84324-046-01L188-00 NC-Pain Relief-84324-046-01

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130384324000619GTIN-13: 0384324000619
EAN-13: 0384324000619
GTIN-12: 384324000619
UPC-A: 384324000619
GTIN storage (14 digits): 00384324000619
L188-00 NC-Pain Relief-84324-046-01.jpg

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84324-04684324-046-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-07-30daily-update2026-08-04 03:33:29

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
Pain Relief Acetaminophen 325 mgACETAMINOPHENNUVICARE LLC49a59b79-b8b4-4bf5-a403-0a14751efc552026-08-03WarningsExact identifier
ndc (package): 84324-046-01
ndc (product): 84324-046
ndc11 (package): 84324004601
spl id: b2b68fd0-c6d1-47ab-b8d1-c89f45c2401a
spl set id: 49a59b79-b8b4-4bf5-a403-0a14751efc55

Reported adverse events (FAERS/openFDA)#

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