Junior Strength Pain Relief

Manufacturer
Capricorn Pharma Inc.
Effective date
2010-07-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:25:20

Label at a glance#

ProductJunior Strength Pain Relief
Active ingredientACETAMINOPHEN
Label structure8 sections

Indications and uses

temporarily relieves minor aches and pains due to: ■ the common cold  ■ flu  ■ headache  ■ temporarily  reduces fever

Dosage and administration

This product does not contain directions or complete warnings for adult use. Do not exceed recommended dose (see overdose warning) ■ find right dose on chart below. If possible, use weight to dose; otherwise, use age ■ dissolve in mouth or chew before swallowing ■ if needed, repeat dose every 4 hours ■ do not use more than 5 times in 24 hours Weight (lb) Under 48 48-59 60-71 72-95 96 and over Age (yr) Under 6 6-8 ...

Label contents#

Full prescribing information#

Active Ingredient(in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Acetaminophen 160mg

Purpose

OTC - PURPOSE SECTION

Pain Reliever/Fever Reducer

Uses

INDICATIONS & USAGE SECTION

temporarily relieves minor aches and pains due to:

■ the common cold 

■ flu 

■ headache 

■ temporarily  reduces fever

Warnings

WARNINGS SECTION

Liver Warning: This product contains acetaminophen. Severe liver damage may occur if your child takes:  
■ more than 5 doses in 24 hours, which is maximum daily amount
■ with other drugs containing acetaminophen

Do not use

OTC - DO NOT USE SECTION

■ with any other product containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if your child has liver disease.

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor or pharmacist before use if your child is taking the blood thinning drug warfarin.

Stop use and ask doctor if

OTC - STOP USE SECTION

■ new symptoms occur  
■ redness or swelling is present
■ pain gets worse or lasts for more than 5 days
■ fever gets worse or lasts for more than 3 days

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Overdose warning:

OVERDOSAGE SECTION

Taking more than the recommended dose (overdose) may cause liver damage. In case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical even if you do not notice any signs or symptoms.

Directions

DOSAGE & ADMINISTRATION SECTION

This product does not contain directions or complete warnings for adult use.
Do not exceed recommended dose (see overdose warning)

■ find right dose on chart below. If possible, use weight to dose; otherwise, use age
■ dissolve in mouth or chew before swallowing
■ if needed, repeat dose every 4 hours
■ do not use more than 5 times in 24 hours

Weight (lb)
Under 48
48-59
60-71
72-95
96 and over
Age (yr)
Under 6
6-8
9-10
11
12
Tablets
Ask a doctor
2
2-1/2
3
4

Other Information

SPL UNCLASSIFIED SECTION

■ Do not use if blister unit is broken or shows signs of tampering.
■ Store between 20-25ºC (68-77ºF). Avoid high humidity. Protect from light.
■ See end panel for lot number and expiration date.

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Crospovidone, D & C red # 7, D & C red # 30, ethylcellulose, FD & C blue # 1, flavor, magnesium stearate, maltodextrin, mannitol, microcrystalline cellulose, modified starch, polysorbate 80, silicon dioxide, sodium lauryl sulfate, sodium starch glycolate, sucralose, talc, triethyl citrate

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Capricorn Pharma
ORIGINAL DEVELOPERS AND MANUFACTURERS
Compare to the active ingredient of Junior Tylenol Meltaways
JUNIOR STRENGTH
Pain Relief
ACETAMINOPHEN - 160mg each
For Children Ages 6-11

See new warnings information

    * Fever Reducer
    * Pain Reliever
    * Contains no Aspirin
    * Melts in your mouth

RAPIDMELT

24 Fast Dissolving Tablets

Grape Flavor
Junior strength Pain Relief Acetaminophen 160mg
Junior strength Pain Relief Acetaminophen 160mg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
477282acetaminophen 160 MG Disintegrating Oral TabletPSN1
477282acetaminophen 160 MG Disintegrating Oral TabletSCD1
477282APAP 160 MG Disintegrating Oral TabletSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
66007-145-022019-10-21C16284748780-1956f9ecf-ce76-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66007-145-01Junior Strength Pain Relief6 in 1 BLISTER PACKTABLET61
66007-145-02Junior Strength Pain Relief4 in 1 CARTONTABLET41

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66007-145JUNIOR STRENGTH PAIN RELIEF (ACETAMINOPHEN) TABLET [CAPRICORN PHARMA INC.]1Legacy NDC, 2 package rows20100728_9fa0eaa3-d9c6-45c8-9613-edf9e50021e9.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ACETAMINOPHENACTIVE INGREDIENT362O9ITL9D1
ACETAMINOPHENACTIVE MOIETY362O9ITL9D1

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66007-14566007-145-01, 66007-145-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACETAMINOPHEN362O9ITL9DACTIB

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
a7e74856-eb57-4153-bae9-008f0cfdbbf99fa0eaa3-d9c6-45c8-9613-edf9e50021e92010-07-26WarningsExact identifier
spl id: a7e74856-eb57-4153-bae9-008f0cfdbbf9
spl set id: 9fa0eaa3-d9c6-45c8-9613-edf9e50021e9

Reported adverse events (FAERS/openFDA)#

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