---
title: "DoctoRx's Optimal Formula, Dry Eye Formula, Ocular Support Softgel, 60 Softge... — FDA record F-0352-2022 | Is It on Recall"
description: "Undeclared fish allergen"
url: https://isitonrecall.com/recall/fda-food-f-0352-2022-doctorx-s-optimal-formula-dry-eye-formula-ocular-support-softgel-60-softgels-dietary-supplement/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# DoctoRx's Optimal Formula, Dry Eye Formula, Ocular Support Softgel, 60 Softgels/Dietary Supplement — FDA record F-0352-2022

Reported terminated

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 30, 2021. 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**: DoctoRx's Optimal Formula, Dry Eye Formula, Ocular Support Softgel, 60 Softgels/Dietary Supplement
- **Reason**: Undeclared fish allergen
- **Classification**: Class II
- **Recalling firm**: Golden Lab LLC
- **Quantity**: 13,079 units
- **Agency-reported status**: Terminated
- **Source record identifier**: F-0352-2022

[Open the official record](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-0352-2022%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 | Lots: D93210669 and E11290344 |

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

## Distribution

Domestic distribution only.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Dec 29, 2021
- **Recall initiation date**: Nov 30, 2021
- **Center classification date**: Dec 23, 2021
- **Termination date**: Mar 15, 2022

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/food/enforcement.json?search=recall_number%3A%22F-0352-2022%22)

## Related records

[Supplements records](https://isitonrecall.com/product/supplements/) [Supplements records](https://isitonrecall.com/category/supplements/) [Golden Lab LLC records](https://isitonrecall.com/brand/golden-lab-llc/)