Active Ingredients
Acetaminophen 325 mg
Regular Strength Pain Relief
FDA Label NDC 71335-1847
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bryant Ranch Prepack for the product Regular Strength Pain Relief (NDC 71335-1847). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, purpose, uses, warnings, otc - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Pain Reliever/Fever Reducer
Uses
- temporarily relieves minor aches and pains
- temporarily reduces fever
Warnings
Liver warning:
This product contains acetaminophen. Severe liver damage may occur if you take
- more than 4,000 mg (12 tablets) of acetaminophen in 24 hours
- with other drugs containing acetaminophen
- 3 or more alcoholic drinks every day while using this product
- with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
- 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
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
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
These could be signs of a serious condition.
If pregnant or breast-feeding,
ask a health professional before use.
Otc - Keep Out Of Reach Of Children
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.
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. Do not take for more than 10 days unless directed by a doctor. - children under 12 years: ask a doctor
Other Information
- TAMPER EVIDENT: Do not use if imprinted seal under cap is missing or broken.
- store at 20⁰C-25⁰C (68⁰F-77⁰F)
Inactive Ingredients
povidone, sodium starch glycolate, starch, stearic acid.
Questions Or Comments?
1-800-540-3765
How Supplied
NDC: 71335-1847-1: 20 Tablets in a BOTTLE
NDC: 71335-1847-2: 100 Tablets in a BOTTLE
NDC: 71335-1847-3: 30 Tablets in a BOTTLE
NDC: 71335-1847-4: 2 Tablets in a BOTTLE
NDC: 71335-1847-5: 6 Tablets in a BOTTLE
NDC: 71335-1847-6: 10 Tablets in a BOTTLE
NDC: 71335-1847-7: 60 Tablets in a BOTTLE
NDC: 71335-1847-8: 90 Tablets in a BOTTLE
NDC: 71335-1847-9: 40 Tablets in a BOTTLE
NDC: 71335-1847-0: 24 Tablets in a BOTTLE
Package Label.Principal Display Panel
Acetaminophen 325 mg. Tablet
Label (Lbl713351847)
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