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Capment

Medically reviewed on March 26, 2018

Dosage form: patch
Ingredients: MENTHOL .041 in 100g, CAPSAICIN .003751 in 100g
Labeler: Original Patch Company Inc
NDC Code: 69650-001

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Capment

Active ingredients:

Capsaicin 0.0375%

Menthol 5.00%

Purpose

Topical Anesthetic

Topical Analgesic

Keep out of reach of children. Consult physician for children under 12.

Uses

For the temporary relief of minor aches and muscle pain associated with arthritis, simple backache, strains, muscle soreness and stiffness.

Warnings
  • Only for external use. Use only as directed or by a health professional.
  • Do not use: on open wounds, cuts, damaged or infected skin as well as in the eyes, mouth, genitals, or any other mucous membranes.
  • Do not cover with bandage.
  • Consult your physician: If pregnant or pain persists or worsens.

Directions

Adults and children 12 and over: Apply patch to affected area 1 to 2 times daily or as directed.

Instructions for Use:

  • Clean and dry affected area
  • Open pouch and remove on patch
  • Remove any protective film and apply directly to affected area of pain
  • Wash hands with soap and water after applying patch
  • Reseal pouch containing unused patches after each use

Other Ingredients:

WATER, GLYCERIN, SODIUM POLYACRYLATE (2500000 MW), POLYSORBATE 80, ALOE VERA LEAF, EDETATE DISODIUM, DIAZOLIDINYL UREA, METHYLPARABEN, IODOPROPYNYL BUTYLCARBAMATE, PROPYLPARABEN

Store in a dry, cool place

Packaging

CAPMENT 
menthol, capsaicin patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69650-001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (MENTHOL) MENTHOL.04   in 100 g
CAPSAICIN (CAPSAICIN) CAPSAICIN.00375   in 100 g
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE 
ACRYLIC ACID/SODIUM ACRYLATE COPOLYMER (1:1; 600 MPA.S AT 0.2%) 
Packaging
#Item CodePackage Description
1NDC:69650-001-1515 PATCH in 1 BOX
1NDC:69650-001-051 g in 1 PATCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other03/24/2015
Labeler - Original Patch Company Inc (079705068)

 
Original Patch Company Inc

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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