US Drug Recall Register
Class II · Moderate risk Terminated Initiated May 4, 2018 (8 years ago)

Naturmetic SPF 50 Sunscreen

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

Why it was recalled

GMP Deviations

What was recalled

Naturmetic SPF 50 Sunscreen (Octinoxate 7.5%, Zinc Oxide 10.5%), 2.0 fl oz/60mL bottles, Fortis BioPharma, Magnolia, TX 77354.

Recalling firm
Milbar Laboratories, Inc.
Origin
CT, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0813-2018

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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