CAPMENT- menthol, capsaicin patch

Capment by

Drug Labeling and Warnings

Capment by is a Prescription medication manufactured, distributed, or labeled by Original Patch Company Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients:

Capsaicin 0.0375%

Menthol 5.00%

Purpose

Topical Anesthetic

Topical Analgesic

KEEP OUT OF REACH OF CHILDREN

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

STORAGE AND HANDLING

Store in a dry, cool place

Packaging

INGREDIENTS AND APPEARANCE

CAPMENT 
menthol, capsaicin patch

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 69650-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	.04   in 100 g
CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM)	CAPSAICIN	.00375   in 100 g

Inactive Ingredients
Ingredient Name	Strength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
ACRYLIC ACID/SODIUM ACRYLATE COPOLYMER (1:1; 600 MPA.S AT 0.2%) (UNII: M4PPW69Y4H)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69650-002-15	15 in 1 BOX
1	NDC: 69650-002-05	1 g in 1 PATCH

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/31/2015

Labeler - Original Patch Company Inc (079705068)