Label: UP AND UP PAIN- camphor, menthol, and methyl salicylate patch

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated April 11, 2022

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  • ACTIVE INGREDIENT

    Active ingredients Purposes

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

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

    Methyl Salicylate 6.3%........................................Topical analgesic

  • PURPOSE

    Uses

    temporarily relieves the minor aches and pains of muscles and joints associated with:

    • sprains
    • simple backache
    • arthirtis
    • strains
    • bruises
  • WARNINGS

    Warnings

    For external use only

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

  • DO NOT USE

    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
  • ASK DOCTOR

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

  • WHEN USING

    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
  • STOP USE

    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
  • PREGNANCY OR BREAST FEEDING

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

  • KEEP OUT OF REACH OF CHILDREN

    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

    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

    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

    Inactive ingredients

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

  • DOSAGE & ADMINISTRATION

    Distributed by:

    Target Corproation

    Minneapolis, MN 55403

    Made in China

  • PRINCIPAL DISPLAY PANEL

    90213

  • INGREDIENTS AND APPEARANCE
    UP AND UP PAIN 
    camphor, menthol, and methyl salicylate patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82442-213
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)12 mg
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL57 mg
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE63 mg
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERYL ROSINATE (UNII: SD112V492J)  
    LANOLIN (UNII: 7EV65EAW6H)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)  
    NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82442-213-605 in 1 CARTON01/11/2022
    11 in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34801/11/2022
    Labeler - Target Corporation (006961700)
    Registrant - United Exchange Corp. (840130579)
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