Pain Reliever

Manufacturer
Kool 'N Fit Inc.
Effective date
2025-11-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:15:59

Label at a glance#

ProductPain Reliever
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL
Label structure10 sections

Storage and handling

Store in a cool dry place

Label contents#

Full prescribing information#

OTHER INFO

STORAGE AND HANDLING SECTION

Store in a cool dry place

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

ALCOHOL SDA-40, AQUA DEIONIZED, USP, BERGAMOT OIL, CITRUS OIL, EUCALYPTUS OIL, JUNIPERBERRY OIL, PINE NEEDLE OIL, MYRISTICA OIL, LAVENDULA OIL, LEMON OIL, PEPPERMINT OIL, ROSEMARY OIL, THYME OIL

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH CHILDREN - IF SWALLOWED GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

DIRECTION

DOSAGE & ADMINISTRATION SECTION

ADULTS AND CHILDREN 2 YEARS OF AGE AND OLDER:

APPLY TO AFFECTED AREA NOT MORE THAN 3 TO 4 TIMES DAILY.

CHILDREN UNDER 2 YEARS OF AGE. DO NOT USE, CONSULT DOCTOR.

WARNING

WARNINGS SECTION

FOR EXTERNAL USE ONLY.

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Camphor 0.20%

Menthol 1.25%

PURPOSE

OTC - PURPOSE SECTION

for the temporary relief of minor aches and pains of muscle and joints asscoiated with simple backache, strains, brusies and sprains.

USE

INDICATIONS & USAGE SECTION

USE ONLY AS DIRECTED.

RECENT MAJOR CHANGES SECTION

COMPLETE ALL CONTENT SECTIONS TO ALIGN WITH PRODUCT PACKAGING

PRODUCT LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Kool N Fit Muscle Pain Relieving sprayKool N Fit Muscle Pain Relieving sprayKOOL N FIT - PAIN RELIEVING SPRAY

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1923699camphor 0.2 % / menthol 1.25 % Topical SprayPSN3
1923699camphor 2 MG/ML / menthol 12.5 MG/ML Topical SpraySCD3
1923699camphor 0.2 % / menthol 1.25 % Topical SpraySY3

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130030141010088GTIN-13: 0030141010088
EAN-13: 0030141010088
GTIN-12: 030141010088
UPC-A: 030141010088
GTIN storage (14 digits): 00030141010088
KOOL N FIT - PAIN RELIEVING SPRAY 8 OZ.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84733-302-01Pain Reliever3785 g in 1 BOTTLESPRAY37853
84733-302-02Pain Reliever59.145 g in 1 BOTTLE, SPRAYSPRAY59.1453
84733-302-04Pain Reliever236.58 g in 1 BOTTLE, SPRAYSPRAY236.583
84733-302-08Pain Reliever118.29 g in 1 BOTTLE, SPRAYSPRAY118.293
84733-302-16Pain Reliever473.17 g in 1 BOTTLESPRAY473.173

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84733-30284733-302-08, 84733-302-04, 84733-302-16, 84733-302-02, 84733-302-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
Pain RelieverCAMPHOR, MENTHOLKool 'N Fit Inc.2253f6bd-5707-b993-e063-6394a90aa74a2025-11-13WarningsExact identifier
ndc (package): 84733-302-01
ndc (package): 84733-302-02
ndc (package): 84733-302-16
ndc (package): 84733-302-08
ndc (package): 84733-302-04
ndc (product): 84733-302
ndc11 (package): 84733030208
ndc11 (package): 84733030201
ndc11 (package): 84733030204
ndc11 (package): 84733030202
ndc11 (package): 84733030216
spl id: 43828e33-3763-a578-e063-6294a90af9ed
spl set id: 2253f6bd-5707-b993-e063-6394a90aa74a

Reported adverse events (FAERS/openFDA)#

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