US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Nov 22, 2024 (2 years ago)

10 Irregular Pigmentation, Accelerator, Pigment Fading Activator, Only Your Rx, Nature +…

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

Why it was recalled

CGMP Deviations: Inconsistency in the water systems.

What was recalled

10 Irregular Pigmentation, Accelerator, Pigment Fading Activator, Only Your Rx, Nature + Science, 1 fl. oz., 30 mL Bottle, For Professional Use Only, Only YourRx Inc., Chatsworth, CA 91311, Made in USA, Onlyyourrx.com.

Recalling firm
Generitech Corporation
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0111-2025

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.