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Aleveer Patch

Generic name: menthol
Dosage form: topical patch
Drug class: Topical rubefacient

Medically reviewed by Drugs.com. Last updated on Jul 22, 2021.

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.

Warnings

For external use only

Use only as directed

Avoid contact with eyes and muccous membranes

Do not cover wit hbandage

Do not use on wounds or damaged skin

Consult physician for children under 12

Do not use if you are allergic to menthol

Stop use and ask doctor if conditions worsen, wymptoms persist for more tahn 7 days or clear up and occur again within a few days or rash, itching or excessive skin irritation occurs

Keep out of reach of children

Menthol 5.00%

Capsaicin 0.0375%

water, glycerine, sodium polyacrylate, polysorbate80, aloe barbadesis leaf juice, EDTA disodium salt, diazolidinyl urea, methylparaben, iodoproynyl butylcabamate, propylparaben

adults and children 12 years and over apply to affected area; change patch 1 to 2 times daily

children under 12 years consult physician before use

how to apply: clean and dry affected area, cut open pouch and remove patch, remove protective film and apply directly to area of pain, apply to affected area not more than 3 times daily, wash hands with soap after applying patch, reseal pouch containing unused patches.

Analgesic/counterirritant

External analgesic

Analgesic/counterirritant

External analgesic

Allever Patch

Aleveer Patch
menthol patch
Product Information
Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:49430-014
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MENTHOL (MENTHOL) MENTHOL 5 g in 100 g
CAPSAICIN (CAPSAICIN) CAPSAICIN .0375 g in 100 g
Inactive Ingredients
Ingredient Name Strength
WATER
GLYCERIN
SODIUM POLYACRYLATE (2500000 MW)
POLYSORBATE 80
ALOE VERA LEAF
EDETATE DISODIUM
DIAZOLIDINYL UREA
METHYLPARABEN
IODOPROPYNYL BUTYLCARBAMATE
PROPYLPARABEN
Packaging
# Item Code Package Description
1 NDC:49430-014-15 100 g in 1 PATCH
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 10/01/2013
Labeler - Pharmaceutics Corporation (079132026)
Pharmaceutics Corporation

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