FDA recall record

Taro Pharmaceuticals U.S.A Kamedis BIO-HERBAL DANDRUFF CARE THERAPEUTIC 2-STEP DANDRUFF CARE recall — FDA D-0134-2017

Subpotent Drug: Out of Specification assay values on stability for the active ingredient, zinc pyrithione.

Class IIIclassification
D-0134-2017official record ID
Nov 16, 2016report date

Recall record at a glance

Official recordD-0134-2017
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmTaro Pharmaceuticals U.S.A., Inc.
Report dateNov 16, 2016
Recall initiation dateMay 26, 2016
Quantity17,100 kits
LocationHawthorne, NY, United States

Official product description

Kamedis BIO-HERBAL DANDRUFF CARE THERAPEUTIC 2-STEP DANDRUFF CARE SYSTEM - Kamedis Bio-Herbal Dandruff Care 0.1% PYRITHIONE ZINC, STEP 1 PRE-TREAT Concentrated Botanical Scalp Lotion (0.1% Pyrithione Zinc) 4.20 FL OZ (125mL) (NDC 51672-2126-0) and STEP 2 CLEANSE Concentrated Botanical Dandruff Shampoo (1.0% Pyrithione Zinc)(0.6.80 FL OZ (200 mL) (NDC 51672-2125-5), Distributed by: Taro Pharmaceuticals U.S.A, Inc. Hawthorne, NY 10532. NDC

Why the product was recalled

Subpotent Drug: Out of Specification assay values on stability for the active ingredient, zinc pyrithione.

Distribution information

Nationwide

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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About this record

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