Gc 102
a966e24f-559c-3249-e053-2a95a90acbc9
34390-5
HUMAN OTC DRUG LABEL
Drug Facts
Composition & Product
Identifiers & Packaging
Description
Acetaminophen 325 mg
Purpose
Pain Reliever/Fever Reducer
Medication Information
Purpose
Pain Reliever/Fever Reducer
Description
Acetaminophen 325 mg
Uses
- temporarily relieves minor aches and pains
- temporarily reduces fever
Section 50565-1
Keep out of reach of children. In case of overdose, get
medical help or contact a Poison Control Center right away.
Quick medical attention is critical for adults as well as for
children even if you do not notice any signs or symptoms.
Warnings
Liver warning: This product contains acetaminophen.
The maximum daily dose of this product is 10 tablets
in 24 hours. Severe liver damage may occur if you take:
- more than 12 tablets (4,000 mg of acetaminophen)
in 24 hours
- with other drugs containing acetaminophen
- 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.
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.
Ask a doctor before use if you have liver disease
Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin.
Stop use and ask a doctor if
- pain gets worse or lasts more than 10 days
- fever gets worse or lasts more than 3 days
- new symptom occur
- redness or swelling is present
These could be signs of a serious condition.
If pregnant or breast-feeding, ask a health professional before use.
Directions
- do not take more than directed
- adults and children 12 years and over: take 2 tablets every 4-6 hours, as needed; not more than 10 tablets in 24 hours
- children under 12 years: ask a doctor
Other Information
- store at 20⁰C-25⁰C (68⁰F-77⁰F)
Active Ingredients
Acetaminophen 325 mg
Inactive Ingredients
povidone, sodium starch glycolate, starch stearic acid.
Principle Display Panel
NDC: 70934-776-90
Structured Label Content
Uses
- temporarily relieves minor aches and pains
- temporarily reduces fever
Section 50565-1 (50565-1)
Keep out of reach of children. In case of overdose, get
medical help or contact a Poison Control Center right away.
Quick medical attention is critical for adults as well as for
children even if you do not notice any signs or symptoms.
Purpose
Pain Reliever/Fever Reducer
Warnings
Liver warning: This product contains acetaminophen.
The maximum daily dose of this product is 10 tablets
in 24 hours. Severe liver damage may occur if you take:
- more than 12 tablets (4,000 mg of acetaminophen)
in 24 hours
- with other drugs containing acetaminophen
- 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.
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.
Ask a doctor before use if you have liver disease
Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin.
Stop use and ask a doctor if
- pain gets worse or lasts more than 10 days
- fever gets worse or lasts more than 3 days
- new symptom occur
- redness or swelling is present
These could be signs of a serious condition.
If pregnant or breast-feeding, ask a health professional before use.
Directions
- do not take more than directed
- adults and children 12 years and over: take 2 tablets every 4-6 hours, as needed; not more than 10 tablets in 24 hours
- children under 12 years: ask a doctor
Other Information
- store at 20⁰C-25⁰C (68⁰F-77⁰F)
Active Ingredients
Acetaminophen 325 mg
Inactive Ingredients
povidone, sodium starch glycolate, starch stearic acid.
Principle Display Panel
NDC: 70934-776-90
Advanced Ingredient Data
Raw Label Data
All Sections (JSON)
Additional Information
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Source: dailymed · Ingested: 2026-02-15T11:59:00.495451 · Updated: 2026-03-14T22:58:50.271611