ApprovalTrail

Natural health product · DIN 02004240

ZOSTRIX HP

Yes: licensed in Canada

The product licence is active. Whether the product is actually on the market is a separate, voluntary notice; the official record shows it.

Licence status Active; licensed April 2, 2008; licence last revised March 18, 2025.
DIN
02004240
Licence holder
Bausch & Lomb Inc.Rochester, New York, United States
Dosage form
Cream
Route
Topical
Licensing route
Transitional DIN
First licensed
April 2, 2008
Licence last revised
March 18, 2025

Medicinal ingredients

Per dosage unit, as licensed.

IngredientAmount
(6E)-N-[(4-Hydroxy-3-methoxyphenyl)methyl]-8-methyl-6-nonenamideCapsicum frutescens - fruit0.075 % (w/w)
(6E)-N-[(4-Hydroxy-3-methoxyphenyl)methyl]-8-methyl-6-nonenamideCapsicum annuum - fruit0.075 % (w/w)

What it is licensed for

The licence’s own wording. Directions, doses, cautions and warnings are on the official record and the label.

  • Used for the (temporary) relief of muscle and joint pain associated with rheumatoid arthritis or osteoarthritis, and pain of tendons and ligaments. Used to relieve skin (cutaneous) pain associated with conditions such as post-herpetic neuralgia and/or diabetic neuropathy.

Non-medicinal ingredients

Purified water; Isopropyl myristate; Glyceryl Monostearate; Cetyl Alcohol; Benzyl Alcohol; Sorbitol; Petrolatum, White

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