---
title: "10 Irregular Pigmentation, Accelerator, Pigment Fading Activator, Only Your R... — FDA record D-0111-2025 | Is It on Recall"
description: "CGMP Deviations: Inconsistency in the water systems."
url: https://isitonrecall.com/recall/fda-drug-d-0111-2025-10-irregular-pigmentation-accelerator-pigment-fading-activator-only-your-rx-nature-science-1-fl-oz-3/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA drug enforcement

# 10 Irregular Pigmentation, Accelerator, Pigment Fading Activator, Only Your Rx, Nature + Science, 1 fl. oz., 30 mL Bo... — FDA record D-0111-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Nov 22, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: 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.
- **Reason**: CGMP Deviations: Inconsistency in the water systems.
- **Classification**: Class II
- **Recalling firm**: Generitech Corporation
- **Quantity**: 77.5lbs
- **Agency-reported status**: Ongoing
- **Source record identifier**: D-0111-2025

[Open the official record](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0111-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot #: 2400017, Exp: 4/30/2026 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

CA

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [California](https://isitonrecall.com/state/california/)

## Dates in the source

- **Report date**: Dec 11, 2024
- **Recall initiation date**: Nov 22, 2024
- **Center classification date**: Dec 5, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0111-2025%22)

## Before changing a medicine

Follow urgent instructions in the current official recall notice. Speak to your pharmacist or prescriber before stopping or changing a prescribed medicine.

Talk to your doctor or pharmacist if you have questions or concerns about your medicine. [FDA medication recall guidance](https://www.fda.gov/drugs/drug-recalls/understanding-drug-recalls-what-know-and-what-do)

## Related records

[Medications records](https://isitonrecall.com/category/medications/) [Generitech Corporation records](https://isitonrecall.com/brand/generitech-corporation/)