PAIN RELIEVING- camphor, menthol, and methyl salicylate patch 
Target Corporation

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.

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Up & Up Pain Relief Patches 60ct 90210

Active ingredients Purposes

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

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

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

Uses

Warnings

For external use only

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

Do not use

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

When using this product

Stop use and ask a doctor if

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

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

Directions

Other information

Inactive ingredients

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

Distributed by

90210

PAIN RELIEVING 
camphor, menthol, and methyl salicylate patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-345
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL131 mg
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC)28.4 mg
Inactive Ingredients
Ingredient NameStrength
METHYL SALICYLATE (UNII: LAV5U5022Y) 144 mg
POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7)  
CALCIUM CARBONATE (UNII: H0G9379FGK)  
ZINC OXIDE (UNII: SOI2LOH54Z)  
NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-345-6060 in 1 BOX03/13/2019
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 finalpart34803/13/2019
Labeler - Target Corporation (006961700)

Revised: 12/2022
Document Id: efe61d7c-20ae-50e7-e053-2995a90af351
Set id: 83ff36dd-9be4-190b-e053-2a91aa0a7ac6
Version: 3
Effective Time: 20221215
 
Target Corporation