---
title: "Rapidol Maximum Strength, Hydrocortisone 1% Anti-Itch Cream, NET WT 2 oz (60g... — FDA record D-0428-2025 | Is It on Recall"
description: "CGMP Deviations"
url: https://isitonrecall.com/recall/fda-drug-d-0428-2025-rapidol-maximum-strength-hydrocortisone-1-anti-itch-cream-net-wt-2-oz-60g-tube-distributed-by-pharma/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Rapidol Maximum Strength, Hydrocortisone 1% Anti-Itch Cream, NET WT 2 oz (60g) Tube, Distributed by: Pharmadel LLC, N... — FDA record D-0428-2025

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 Apr 24, 2025. 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**: Rapidol Maximum Strength, Hydrocortisone 1% Anti-Itch Cream, NET WT 2 oz (60g) Tube, Distributed by: Pharmadel LLC, New Castle, DE, 19720, NDC 55758-420-02, UPC 8 10096 77158 2.
- **Reason**: CGMP Deviations
- **Classification**: Class II
- **Recalling firm**: KENIL HEALTHCARE PRIVATE LIMITED
- **Quantity**: 10,000 Tubes
- **Agency-reported status**: Terminated
- **Source record identifier**: D-0428-2025

[Open the official record](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0428-2025%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 SP26A, Exp: 09/30/2026 |

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

## Distribution

DE and NC

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

- [Delaware](https://isitonrecall.com/state/delaware/)
- [North Carolina](https://isitonrecall.com/state/north-carolina/)

## Dates in the source

- **Report date**: May 28, 2025
- **Recall initiation date**: Apr 24, 2025
- **Center classification date**: May 19, 2025
- **Termination date**: Feb 19, 2026

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-0428-2025%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/) [KENIL HEALTHCARE PRIVATE LIMITED records](https://isitonrecall.com/brand/kenil-healthcare-private-limited/)