Pain Relief Patch

Manufacturer
CDMA, Inc. | Foshan Aqua Gel Biotech Co., Ltd.,
Effective date
2025-07-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:07:06

Label at a glance#

ProductPain Relief Patch
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE
Label structure13 sections

Indications and uses

Temporary relief of minor aches and pains of muscles and joints: arthritis, simple backache, muscle strains, muscle sprains, and bruises.

Dosage and administration

Adults and children 12 years of age and over: Clean and dry affected area, free of lotions, ointments and creams. Remove patch from film, apply to affected area. Do not use more than one patch in an 8 hour period. Repeat as necessary. Maximum 3 patches per day. Discard patch after single use. Reseal pouch after opening. Children under 12 years of age: Consult a physician.

Storage and handling

Store in a clean, dry place outside of direct sunlight. Protect from excessive moisture.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 3.1% - Topical analgesic

Menthol 6.0% - Topical analgesic

Methyl Salicylate 10.0% - Topical analgesic

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Uses

INDICATIONS & USAGE SECTION

Temporary relief of minor aches and pains of muscles and joints: arthritis, simple backache, muscle strains, muscle sprains, and bruises.

Warnings

WARNINGS SECTION

For external use only.

Allergy alert: If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and over: Clean and dry affected area, free of lotions, ointments and creams. Remove patch from film, apply to affected area. Do not use more than one patch in an 8 hour period. Repeat as necessary. Maximum 3 patches per day. Discard patch after single use. Reseal pouch after opening.

Children under 12 years of age: Consult a physician.

Other Information

STORAGE AND HANDLING SECTION

Store in a clean, dry place outside of direct sunlight. Protect from excessive moisture.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Hydrogenated poly

Pentaerythrityl tetra-di-t-butyl hydroxyhydrocinnamate

Petroleum

Styrene/isoprene copolymer

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional before use.

OTC - STOP USE SECTION

Stop use and consult a doctor if rash, itching or excessive skin irritation develops, condition worsens, symptoms last more than 7 days or clear up and occur again within a few days.

OTC - DO NOT USE SECTION

Do not use more than one patch on your body at a time, on wounds or damaged skin, with a heating pad, or if you are allergic to any ingredients of this product.

OTC - WHEN USING SECTION

When using this product: Use only as directed, avoid contact with eyes, mucous membranes or rashes, do not bandage tightly, do not use at the same time as other topical analgesics.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1793147camphor 3.1 % / menthol 6 % / methyl salicylate 10 % Medicated PatchPSN1
1793147camphor 0.031 MG/MG / menthol 0.06 MG/MG / methyl salicylate 0.1 MG/MG Medicated PatchSCD1
1793147camphor 3.1 % / menthol 6 % / methyl salicylate 10 % Medicated PatchSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83324-255-60Pain Relief Patch60 in 1 PACKAGEPATCH601

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83324-25583324-255-60

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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 PatchCAMPHOR, METHYL SALICYLATE, MENTHOLCDMA, Inc.da1ec2fe-cc37-4126-90a8-6eb4b8f2e57b2025-07-09WarningsExact identifier
ndc (package): 83324-255-60
ndc (product): 83324-255
ndc11 (package): 83324025560
spl id: 398479a1-bca6-fcd9-e063-6294a90ad620
spl set id: da1ec2fe-cc37-4126-90a8-6eb4b8f2e57b

Reported adverse events (FAERS/openFDA)#

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