Pain Relieving

Manufacturer
Target Corporation
Effective date
2022-12-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:52:27

Label at a glance#

ProductPain Relieving
Active ingredientMENTHOL, CAMPHOR (SYNTHETIC)
Label structure14 sections

Storage and handling

Other information store at room temperature 20-25°C (68-77°F) avoid strong product in direct sunlight protect product from excessive moisture

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients Purposes

Camphor 1.2%................................................Topical analgesic

Menthol 5.7%..................................................Topical analgesic

Methyl salicylate 6.3%.....................................Topical analgesic

OTC - PURPOSE SECTION

Uses

  • temporarily relieves the minor aches and pains of muscles and joints associated with:
  • sprains
  • simple backache
  • bruises
  • arthritis
  • strains

WARNINGS SECTION

Warnings

For external use only

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

OTC - DO NOT USE SECTION

Do not use

  • on wounds or damaged skin
  • with a heating pad
  • if you are allergic to any ingredients of this product
  • on a child under 12 years of age with arthritis-like conditions

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have redness over the affected area

OTC - WHEN USING SECTION

When using this product

  • do not use otherwise than as directed
  • avoid contact with eyes, mucous membranes or rashes
  • do not bandage tightly
  • discontinue use at least 1 hour before a bath or shower
  • do not use immediately after a bath or shower

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • redness is present or irritation or rash develops
  • condition worsens or symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use

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

INDICATIONS & USAGE SECTION

Directions

  • adults and children 12 years of age and older:
  • clean and dry affected area
  • remove patch from film
  • apply to affected area no more than 3 to 4 times daily
  • do not water patch for more than 8 hours
  • children under 12 years of age: consult a doctor

STORAGE AND HANDLING SECTION

Other information

  • store at room temperature 20-25°C (68-77°F)
  • avoid strong product in direct sunlight
  • protect product from excessive moisture

INACTIVE INGREDIENT SECTION

Inactive ingredients

butylated hydroxytoluene, glyceryl rosinate, natural rubber, polybutene, polyisobutylene, precipated calcium carbonate, sorbitan stearate, tocopherol acetate, ys resin, zinc oxide

DOSAGE & ADMINISTRATION SECTION

Distributed by

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

9021090210

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11673-345-602024-01-30C16284748780-11030e365-0836-111a-e063-dadaa90a10e2Up & Up Pain Relief Patches 60ct 90210

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11673-345-60Pain Relieving60 in 1 BOXPATCH603
11673-345-60Pain Relieving1 in 1 PATCHPATCH13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-345PAIN RELIEVING (CAMPHOR, MENTHOL, AND METHYL SALICYLATE) PATCH [TARGET CORPORATION]3Legacy NDC, 2 package rows20221217_83ff36dd-9be4-190b-e053-2a91aa0a7ac6.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11673-34511673-345-60

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 · Source PDF

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
efe61d7c-20ae-50e7-e053-2995a90af35183ff36dd-9be4-190b-e053-2a91aa0a7ac62022-12-15WarningsExact identifier
spl id: efe61d7c-20ae-50e7-e053-2995a90af351
spl set id: 83ff36dd-9be4-190b-e053-2a91aa0a7ac6

Reported adverse events (FAERS/openFDA)#

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