Extra Strength Taminol Acetaminophen

Manufacturer
VIVA PHARMACEUTICAL INC
Effective date
2023-11-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:17:52

Label at a glance#

ProductExtra Strength Taminol Acetaminophen
Active ingredientACETAMINOPHEN
Label structure7 sections

Indications and uses

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

Dosage and administration

■ do not take more than directed (see overdose warning) Adults and chiledren 12 years and over  ■ take two caplets every 6 hour while symptoms last  ■ do not take more than 8 caplets in 24hours unless directed by a doctor  ■ do not take more than 10 days unless directed by a doctor  Children under 12 years  ■ ask a doctor

Label contents#

Full prescribing information#

Drug Facts

SPL UNCLASSIFIED SECTION

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Acetaminophen 500mg

Purposes

OTC - PURPOSE SECTION

Pain reliever/Fever reducer

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

Liver warning: This product conatins acetaminophen.Severe liver damage may occur if yo take ■ more than 4,000 mg of acetaminophen in 24hr ■ with other drug conating acetaminophen ■ 3 or more alcholic drinks everyday 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.

Do not use 

OTC - DO NOT USE SECTION

■with any other drug containg acetaminophen (prescription or non prescription).If you are not sure whether a drug contains acetmniophen.ask doctor or pharmacist. ■ if you are ailergic to acetaminophen or any inactive ingrident in this product.

Aska doctor before use if you have

OTC - ASK DOCTOR SECTION

liver disease

Ask a doctor or pharmacist before use if 

OTC - ASK DOCTOR/PHARMACIST SECTION

you are taking blood thinner

Stop use and ask a doctor if 

OTC - STOP USE SECTION

■ pain get worse or last more than 10 days ■ fever gets worse or lasts more than 3 days condition ■ new sympton occurs ■ redness or swelling present 

If pregnancy or breast-feeding , 

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a healthcare professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Overdose warning: In case of overdose, get medical help or contact a poison control center (1-800-222-1222) right away , 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 chiledren 12 years and over

 ■ take two caplets every 6 hour while symptoms last

 ■ do not take more than 8 caplets in 24hours unless directed by a doctor

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

 Children under 12 years ■ ask a doctor

Other information

SPL UNCLASSIFIED SECTION

■ store at 20°-25°C (68°-77°F)

Inactive ingredients 

INACTIVE INGREDIENT SECTION

Crospovidone , microcrystalline cellulose , Stearic acid , Silicon dioxide

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label0Label0

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52524-000052524-0000-1

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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
1ab22dcb-c3b7-d977-e063-6294a90a06643ef05975-5d96-44db-a786-afec2ebcf11d2024-06-12WarningsExact identifier
spl set id: 3ef05975-5d96-44db-a786-afec2ebcf11d

Reported adverse events (FAERS/openFDA)#

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