Kalaya Pain Relief

Manufacturer
Avaria Health & Beauty Corp
Effective date
2025-10-08
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:38:43

Label at a glance#

ProductKalaya Pain Relief
Active ingredientMENTHOL, CAMPHOR (SYNTHETIC), METHYL SALICYLATE
Label structure10 sections

Indications and uses

Provides penetrating pain relief for the temporary relief of minor aches and pains of muscles and joints 

Dosage and administration

Adults and children 12 years and over: Spray evenly onto affected areas no more than 3 to 4 times daily. Apply spray to affected areas and allowed to dry or thoroughly massage until penetrated.  Wash hands with soap and water after use.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 10%, 

Menthol 8%, 

Methyl salicylate 25%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

Provides penetrating pain relief for the temporary relief of minor aches and pains of muscles and joints 

Warnings

WARNINGS SECTION


For External Use Only. Flammable. Keep away from heat or flame.
Do not Use
• on wounds or damaged skin
• with a heating pad
• on a child under 12 years of age with arthritis-like conditions

When using this product avoid contact with eyes or mucous membranes, do not bandage tightly 

Stop use and ask a doctor if condition worsen or symptoms persist more than 7 days, symptoms clear up and occur again within a few days

excessive skin irritation occurs.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years and over: Spray evenly onto affected areas no more than 3 to 4 times daily. Apply spray to affected areas and allowed to dry or thoroughly massage until penetrated.  Wash hands with soap and water after use.

Other information

SPL UNCLASSIFIED SECTION

Store at 59°F - 77°F

Inactive ingredients

INACTIVE INGREDIENT SECTION

Alcohol Denat., Cannabis Sativa Seed Oil, Citric Acid, Eucalyptus Globulus Leaf Oil, Mentha Piperita (Peppermint) Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil

Questions or comments?

SPL UNCLASSIFIED SECTION

Call toll-free 1.888.829.7165

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2535738camphor 10 % / menthol 8 % / methyl salicylate 25 % Topical SprayPSN5
2535738camphor 100 MG/ML / menthol 80 MG/ML / methyl salicylate 250 MG/ML Topical SpraySCD5
2535738camphor 10 % / menthol 8 % / methyl salicylate 25 % Topical SpraySY5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43493-0007-0Kalaya Pain Relief60 mL in 1 BOTTLE, SPRAYLIQUID605

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43493-000743493-0007-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42024-10-17full-release2026-06-01 00:28:40

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
Kalaya Pain ReliefMETHYL SALICYLATE, MENTHOL, CAMPHORAvaria Health & Beauty Corpe2452c4b-2548-497f-828b-5d960402522a2025-10-08WarningsExact identifier
ndc (package): 43493-0007-0
ndc (product): 43493-0007
ndc11 (package): 43493000700
spl id: 40a7bf23-d763-3c50-e063-6294a90abaa0
spl set id: e2452c4b-2548-497f-828b-5d960402522a

Reported adverse events (FAERS/openFDA)#

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