FDA.reportPublic FDA data

Up and Up Pain

Manufacturer
Target Corporation | United Exchange Corp.
Effective date
2024-12-20
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:47:56

Label at a glance#

ProductUp and Up Pain
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE
Label structure14 sections

Storage and handling

Other information store at room temperature 20-25°C (68-77°F) avoid storing 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
  • arthirtis
  • strains
  • bruises

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 wear patch for more than 4 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 storing product in direct sunlight
  • protect product from excessive moisture

INACTIVE INGREDIENT SECTION

Inactive ingredients

glyceryl rosinate, lanolin, natural latex rubber, petrolatum, polyisobutylene, zinc oxide

DOSAGE & ADMINISTRATION SECTION

Distributed by:

Target Corproation

Minneapolis, MN 55403

Made in China

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

9021390213

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
853260camphor 1.2 % / menthol 5.7 % / methyl salicylate 6.3 % Medicated PatchPSN3
853260camphor 0.012 MG/MG / menthol 0.057 MG/MG / methyl salicylate 0.063 MG/MG Medicated PatchSCD3
853260camphor 1.2 % / menthol 5.7 % / methyl salicylate 6.3 % Medicated PatchSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82442-213-60Up and Up Pain5 in 1 CARTONPATCH53
82442-213-60Up and Up Pain1 in 1 PATCHPATCH13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82442-213UP AND UP PAIN (CAMPHOR, MENTHOL, AND METHYL SALICYLATE) PATCH [TARGET CORPORATION]3Legacy NDC, 2 package rows20241222_d6e4da17-427b-fc0f-e053-2995a90a9fdd.zip

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
82442-21382442-213-60

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
NATURAL LATEX RUBBER2LQ0UUW8INIACT
ZINC OXIDESOI2LOH54ZIACT
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB
MENTHOLL7T10EIP3AACTIB
GLYCERYL ROSINATESD112V492JIACT
LANOLIN7EV65EAW6HIACT
PETROLATUM4T6H12BN9UIACT
POLYISOBUTYLENE (1000 MW)5XB3A63Y52IACT
METHYL SALICYLATELAV5U5022YACTIB

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
29bc7bc0-edca-4352-e063-6294a90aedb5d6e4da17-427b-fc0f-e053-2995a90a9fdd2024-12-20WarningsExact identifier
spl id: 29bc7bc0-edca-4352-e063-6294a90aedb5
spl set id: d6e4da17-427b-fc0f-e053-2995a90a9fdd

Reported adverse events (FAERS/openFDA)#

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