CETAFEN

Manufacturer
A-S Medication Solutions
Effective date
2018-08-15
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-02 00:52:35

Label at a glance#

ProductCETAFEN
Active ingredientACETAMINOPHEN
Label structure14 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient (in each tablet): Acetaminophen 325mg

INDICATIONS & USAGE SECTION

Uses:

Temporarily relieves minor aches and pains due to:

  • headache
  • muscular aches
  • backache
  • minor arthritis pain
  • the common cold
  • toothache
  • menstrual cramps

Temporarily reduces fever

WARNINGS SECTION

Warnings:

Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take:

  • more than 8 tablets in 24 hours, which is the maximum daily amount
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks every day while using this product

OTC - DO NOT USE SECTION

Do not use with any other drug containing acetaminophen (prescription or non-prescription)

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor or pharmacist before use if:

  • you are taking the blood thinning drug warfarin
  • you do not know if other drugs you are taking contain acetaminophen

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have liver disease

OTC - STOP USE SECTION

Stop use and ask a doctor if:

  • new symptom occur
  • redness or swelling is present
  • fever worsens or lasts for more than 3 days
  • pain worsens or lasts for more than 10 days

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: Taking more than the recommended dose (overdose) may cause liver damage. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms. In case of overdose, get medical help or contact Poison Control Center right away. 1-800-222-1222

DOSAGE & ADMINISTRATION SECTION

Directions: Do not take more than directed

Adults and children 12 year of age and over:

  • take 2 tables every 4 to 6 hours while symptoms persist
  • do not take more than 8 tablets in 24 hours unless directed by a doctor

Children under 12 years of age: do not use; this will provide more than the recommended dose (overdose) for children under 12 years of age and may cause liver damage

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Microcrystalline Cellulose, Povidone, Sodium Starch Glycolate, Starch, Stearic Acid

HOW SUPPLIED

HOW SUPPLIED SECTION

Product: 50090-3140

NDC: 50090-3140-0 2 TABLET in a PACKET / 500 in a BOX, UNIT-DOSE

ACETAMINOPHEN

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label Image
Label Image

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50090-314050090-3140-0
50332-0103

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
f4b4a6e4-b774-4740-9c66-5ac7b56051a3e012d671-4769-4164-930f-001422d02e222018-08-15WarningsExact identifier
spl id: f4b4a6e4-b774-4740-9c66-5ac7b56051a3
spl set id: e012d671-4769-4164-930f-001422d02e22

Reported adverse events (FAERS/openFDA)#

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