Pharbetol

Manufacturer
St. Mary's Medical Park Pharmacy
Effective date
2019-11-25
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 23:57:17

Label at a glance#

ProductPharbetol Regular strength
Active ingredientACETAMINOPHEN
Label structure9 sections

Indications and uses

Temporarily relieves minor aches and pains due to the common cold headache backache minor pain of arthritis toothache muscular aches 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 while symptoms last. Do not take more than 12 tablets in 24 hours. Children 6 to under 12 years Take 1 tablet every 4 to 6 while symptoms last. Do not take more than 5 tablets in 24 hours. Children under 6 years Do not use adult regular strength products in childern under 6 ...

Storage and handling

Tamper Evident: do not use if imprinted safety seal under cap is broken or missing store between 20-25°C (68-77°F) use by expiration date on package

Label contents#

Full prescribing information#

Active ingredient (per tablet)

OTC - ACTIVE INGREDIENT SECTION

Acetaminophen 325mg

Purpose

OTC - PURPOSE SECTION

Pain reliever/Fever reducer

Uses

INDICATIONS & USAGE SECTION

  • Temporarily relieves minor aches and pains due to
    • the common cold
    • headache
    • backache
    • minor pain of arthritis
    • toothache
    • muscular aches
    • menstrual cramps
  • Temporarily reduces fever

Warnings

WARNINGS SECTION

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

  • Adult takes more than 12 tablets in 24 hours, which is the maximum daily amount
  • Child takes more than 5 doses in 24 hours
  • Taken with other drugs containing acetaminophen
  • Adult has 3 or more alcoholic drinks every day while using this product

Do not use

OTC - DO NOT USE SECTION

  • 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

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

liver disease.

Ask a doctor or pharmacist before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

taking the blood thinning drug warfarin.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Pain gets worse or lasts more than 10 days in adults and children
  • 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 sign of a serious condition.

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of the reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Overdose warning:

OVERDOSAGE SECTION

Taking more than the recommended dose (overdose) may cause liver damage. In the case of accidental overdose, get medical help or contact a Poison Control Center right away.

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 while symptoms last.
Do not take more than 12 tablets in 24 hours.
Children 6 to under 12 years
Take 1 tablet every 4 to 6 while symptoms last.
Do not take more than 5 tablets in 24 hours.
Children under 6 years
Do not use adult regular strength products in childern under 6 years of age; this will provide more than the recommended dose (overdose) and may cause liver damage.

Other information

STORAGE AND HANDLING SECTION

  • Tamper Evident: do not use if imprinted safety seal under cap is broken or missing
  • store between 20-25°C (68-77°F)
  • use by expiration date on package

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Povidone, pregelatinized starch, sodium starch glycolate, stearic acid.

Questions?

OTC - QUESTIONS SECTION

Adverse drug event call: (866) 562-2756

Acetaminophen 325mg St. Mary's Medical Park Pharmacy

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ACETACET

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60760-449-50EA - Each60760-44905b69534-d8c1-4178-b03f-620f3c326f4812016-05-16
16103-353-07EA - Each16103-353be19f1cb-5a83-4ab8-a81c-dbc7b6c366b312013-05-02
16103-353-08EA - Each16103-353d0efd342-8f78-4b8b-b2ab-963c13f461bf12013-05-02
16103-353-11EA - Each16103-353239e09b4-a5bc-4312-a3cc-d82250536ba312013-05-02

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60760-44960760-449-50
16103-353

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.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Pharbetol Regular strengthACETAMINOPHENPharbest Pharmaceuticals, Inc.e0a39957-d918-4125-88f9-0e550b976fa12025-12-24WarningsExact identifier
ndc (product): 16103-353
9834903a-c25e-42ab-e053-2a95a90ae9c13115c246-cc53-3946-e054-00144ff88e882019-11-25WarningsExact identifier
spl id: 9834903a-c25e-42ab-e053-2a95a90ae9c1
spl set id: 3115c246-cc53-3946-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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