Pain Relief Roll On

Manufacturer
Eagle Labs Inc
Effective date
2026-01-14
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:33:02

Label at a glance#

ProductPain Relief Roll On
Active ingredientMENTHOL, CAMPHOR (SYNTHETIC), CAPSAICIN
Label structure11 sections

Indications and uses

For the temporary relief of aches and pains of muscles and joints associated with arthritis, backaches, strains or sprains

Dosage and administration

Adults and Children over 12 years old: Apply to afected area - do not apply more than 4 times daily. Children 12 years or younger: consult a doctor

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 6%

Camphor 5%

Capsaicin 0.025%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses:

INDICATIONS & USAGE SECTION

For the temporary relief of aches and pains of muscles and joints associated with arthritis, backaches, strains or sprains

Warnings

WARNINGS SECTION

For External use only

When using this product

OTC - WHEN USING SECTION

Use only as directed. Avoid contact with eyes or mucous membranes. Do not apply directly to wounds or damaged skin. Do not use in combination with other ointments, creams, or sprays. Wash hand with cool water after each uyse. Do not use with a heating pad or device.

Stop usage immediately and ask a doctor if:

OTC - STOP USE SECTION

Condition worsens or symptoms persist for more than 7 days

If pregnant or breast-feeding:

OTC - PREGNANCY OR BREAST FEEDING SECTION

Ask a health professional before use

Keep out of reach of children:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If ingested get medical help or contact Poison control center immediately: 1-800-222-1222

Directions:

DOSAGE & ADMINISTRATION SECTION

Adults and Children over 12 years old: Apply to afected area - do not apply more than 4 times daily. Children 12 years or younger: consult a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Citrus Fiber, Dimethicone, Isopropyl Alcohol, Jojoba Oil, Phenoxyethanol, Simethicone, Water

Insta Eaze: Roll the Pain Away

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Insta Eaze Roll the Pain AwayInsta Eaze Roll the Pain Away

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2610122camphor 5 % / capsaicin 0.025 % / menthol 6 % Topical SolutionPSN4
2610122camphor 50 MG/ML / capsaicin 0.25 MG/ML / menthol 60 MG/ML Topical SolutionSCD4
2610122camphor 5 % / capsaicin 0.025 % / menthol 6 % Topical SolutionSY4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
473d070d-1c38-488e-b991-c4d1bf45aab8Product name120210201

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79804-282-032024-04-16C16284748780-11030e365-4080-111a-e063-dadaa90a10e2Pain Relief Roll On
79804-282-032024-01-30C16284748780-11030e365-4080-111a-e063-dadaa90a10e2Pain Relief Roll On

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79804-282-03Pain Relief Roll On87 g in 1 PACKAGELIQUID874

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
79804-28279804-282-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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 Relief Roll OnTOPICAL ANALGESICEagle Labs Inc2380a400-062a-4a8d-a594-a2e0972190442026-01-14WarningsExact identifier
ndc (package): 79804-282-03
ndc (product): 79804-282
ndc11 (package): 79804028203
spl id: 485aeef9-80db-6a7b-e063-6394a90a1477
spl set id: 2380a400-062a-4a8d-a594-a2e097219044

Reported adverse events (FAERS/openFDA)#

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