The Recall Desk
LowFDA (Drugs)·D-1380-2012·Announced 2012-06-20

Quadrant Chemical Recalls Subpotent DermaZinc Spray Zinc Pyrithione Product

Quadrant Chemical Corporation is recalling DermaZinc Spray because the product is subpotent and does not meet the labeled 0.25% zinc pyrithione level.

What this means for you

Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.

Our severity reasoning: The recall is classified as FDA Class III, which by definition is unlikely to cause adverse health consequences, fitting the Low severity criteria for minor labeling or potency issues without reported harm.

Plain-English summary

Quadrant Chemical Corporation is recalling DermaZinc Spray, 0.25% zinc pyritione, topical OTC, 4 fl oz bottle. The product is distributed by Dermallogix Partners, Inc. in Scarborough, ME.

The firm is recalling the product because it is subpotent and does not meet the labeled 0.25% zinc pyrithione level. The recall involves 4,800 bottles of Lot 022110-01, which were distributed in Maine.

Consumers who have this product should stop using it and contact the recalling firm for instructions on how to return or dispose of the product.

The recalled product

Product
DermaZinc Spray, 0.25% zinc pyritione, topical OTC, 4 fl oz bottle Distributed By: Dermallogix Partners, Inc. Scarborough, ME 04070
Manufacturer
Quadrant Chemical Corporation
Category
Drug — Topical OTC
Hazard
Affected units
4,800

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Lot 022110-01

Distribution

Distributed in 1 state:

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