HIGHFDA DRUG

470 Doctor D. Schwab Controlling Cream Tubes Recalled for CGMP Deviations

Doctor D. Schwab recalled 470 tubes of Controlling Cream after discovering CGMP deviations in production. The cream, which contains benzoyl peroxide, may not meet required safety standards. Consumers should stop using the product immediately and contact CA BOTANA for further guidance.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
October 10, 2025
Status
ACTIVE
Severity
7/10

Quick Facts at a Glance

Recall Date
October 10, 2025
Hazard Level
HIGH
Brands
Doctor D. Schwab, CA-BOTANA
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
5 states
At-Risk Groups
GENERAL

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Doctor D. Schwab, CA-BOTANA
Product type
Benzoyl Peroxide Cream
Model numbers
D54066
UPC codes
35192-017, 35192-017-05
Sold at
Multiple Retailers
Where affected
CA, CO, FL, PR, WA

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    October 10, 2025

  2. Reported by FDA DRUG

    December 3, 2025

  3. RecallRadar source check

    April 18, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

CGMP Deviations

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact CA BOTANA International, Inc. or your healthcare provider for guidance. Notification method: Letter

About This Product

Doctor D. Schwab Controlling Cream is a topical treatment designed to help manage acne with an active ingredient of benzoyl peroxide. Consumers often buy this product to treat and prevent breakouts, particularly in teens and adults dealing with acne issues.

Why This Is Dangerous

The recall occurred due to CGMP deviations, which suggest that the manufacturing practices may not have met the required safety and quality standards. This could lead to contamination or ineffective treatment for users.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Users of the product may experience skin irritation or ineffective treatment due to the potential safety deviations. Immediate action is required to avoid health risks.

Practical Guidance

How to identify if yours is affected

  1. Check the tube for the lot code D54066.
  2. Verify the NDC number 35192-017-05 on the product packaging.
  3. Confirm the expiration date of May 31, 2027.

Where to find product info

The lot code and NDC number are typically located on the back or bottom of the tube packaging.

What timeline to expect

Expect a refund or replacement processing time of approximately 4-6 weeks.

If the manufacturer is unresponsive

  • Document all communication attempts with CA BOTANA.
  • Reach out to your healthcare provider for additional support if necessary.
  • File a complaint with the FDA if the company does not respond.

How to prevent similar issues

  • Always check for recalls before purchasing health and personal care products.
  • Look for certifications indicating adherence to safety standards when choosing topical treatments.
  • Read customer reviews for insights on product safety and efficacy before buying.

Documentation advice

Keep records of your purchase receipt, any correspondence with the company, and photos of the product.

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Product Details

Product Name: Doctor D. Schwab Controlling Cream Active Ingredient: Benzoyl Peroxide 2.7% NDC: 35192-017-05 Lot Code: D54066 Expiration Date: May 31, 2027 Distributed in: California, Colorado, Florida, Puerto Rico, Washington

Reported Incidents

No injuries or incidents have been reported.

Key Facts

  • Contains Benzoyl Peroxide 2.7%
  • NDC 35192-017-05 for identification
  • Lot Code D54066, exp 5/31/2027
  • Distributed in CA, CO, FL, PR, WA

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
7/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
D54066
UPC Codes
35192-017
35192-017-05
Affected States
CA, CO, FL, PR, WA
Report Date
December 3, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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