PROFOOT PAIN RELIEF PATCHES- camphor, menthol, methyl salicylate 
Profoot, Inc.

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Profoot Pain Relief Patches

Active ingredients

Camphor 1.2%

Menthol 5.7%

Methyl salicylate 6.3%

Purpose

Topical Analgesic

Topical Analgesic

Topical Analgesic

Uses For temporary relief of minor aches & pains of muscles & joints associated with:

•arthritis •strains •bruises •sprains

Warnings

For external use only

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

Do not use

• on wounds or damaged skin • with a heating pad • if you are allergic to any of the ingredients of

this product

When using this product

• use only as directed • avoid contact with the eyes, mucous membranes or rashes • do not

bandage tightly

Stop use and ask a doctor if

• rash, itching or excessive skin irritation develops • condition worsens •symptoms persist

for more than 7 days • symptoms clear up and occur again within a few days

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

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control

Center right away

Directions

Adults and children 12 years of age and over:

• clean and dry affected area • remove patch from film • apply to affected area not more

than 3-4 times daily • remove patch from skin after at most 8 hours

Children under 12 years of age: consult a doctor

Other information

• avoid storing in direct sunlight • protect product from excessive moisture

Inactive ingredients hydrogenated poly, pentaerythrityl tetra-di-t-butyl Hydroxyhydrocinnamate, white mineral oil, styrene/Isoprene copolymer

Questions or comments? Email cservice@profoot.co

Label InnerLabel

PROFOOT PAIN RELIEF PATCHES 
camphor, menthol, methyl salicylate kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:29784-601
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:29784-601-011 in 1 KIT10/12/2023
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 PATCH 0.36 g
Part 21 PATCH 1.3 g
Part 1 of 2
PROFOOT 
camphor, menthol, methyl salicylate patch
Product Information
Item Code (Source)NDC:29784-121
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE63 mg  in 1 g
CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)12 mg  in 1 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL57 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
STYRENE/ISOPRENE/STYRENE BLOCK COPOLYMER (UNII: K7S96QM8DV)  
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)  
MINERAL OIL (UNII: T5L8T28FGP)  
HYDROGENATED C6-20 POLYOLEFIN (100 CST) (UNII: 39EYQ1W9RB)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
11 in 1 KIT
1NDC:29784-121-360.36 g in 1 PATCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01710/12/2023
Part 2 of 2
PROFOOT 
camphor, menthol, methyl salicylate patch
Product Information
Item Code (Source)NDC:29784-122
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)12 mg  in 1 g
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL57 mg  in 1 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE63 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
MINERAL OIL (UNII: T5L8T28FGP)  
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)  
HYDROGENATED C6-20 POLYOLEFIN (100 CST) (UNII: 39EYQ1W9RB)  
STYRENE/ISOPRENE/STYRENE BLOCK COPOLYMER (UNII: K7S96QM8DV)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
12 in 1 KIT
1NDC:29784-122-361.3 g in 1 PATCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01710/12/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01710/12/2023
Labeler - Profoot, Inc. (107570900)

Revised: 10/2023
Document Id: 0777293c-73f6-8802-e063-6294a90a4b87
Set id: 06f82bde-41a1-35f6-e063-6394a90a6437
Version: 2
Effective Time: 20231011
 
Profoot, Inc.