US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 28, 2014 (12 years ago)

Dermatend Ultra, mole, wart and skin tag remover, For external use only, Ingredient…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Labeling: Labeling Bears Unapproved Claims; Dermatend is not FDA approved and therefore has not been shown to be safe and effective for the uses suggested in the labeling.

What was recalled

Dermatend Ultra, mole, wart and skin tag remover, For external use only, Ingredient: Distilled Water, Sanguinaria Canadensis, Vegetable Glycerin, Butter of Zinc, Germall Plus, 0.34 OZ (10g) container, Solace International, Inc., Reno, NV 89509, USA

Recalling firm
Solace International Inc
Origin
NV, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1586-2014

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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