Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Drug
Medications & Supplements/Topical Products

Elroselabs Inc.: Conzerol and Molleave Products Recalled for Manufacturing Quality Issues

Agency Publication Date: April 6, 2018
Share:
Sign in to monitor this recall

Summary

Elroselabs Inc. is recalling Conzerol zero molluscum contagiosum Topical Cream, Molleave (2 oz), and Conzerol (antipoxin) H2O2 Gel (1.5 oz) because they were manufactured under conditions that did not meet Current Good Manufacturing Practice (cGMP) standards. These deviations mean the firm cannot guarantee the products were made with the necessary quality and safety controls. Consumers should contact their healthcare provider or pharmacist for guidance and return any unused portions of these topical skin treatments to the place of purchase for a refund.

Risk

The recall is due to manufacturing process failures that could affect the safety, purity, and quality of the medications. While no specific injuries are reported, using topical treatments produced with manufacturing deviations may lead to skin irritation or ineffective treatment of conditions like molluscum contagiosum.

What You Should Do

  1. Check your medicine cabinet for Conzerol zero molluscum contagiosum Topical Cream (0.78 oz / 22g), Molleave (2 oz bottle), or Conzerol (antipoxin) H2O2 Gel (1.5 oz tube).
  2. Confirm if your product is affected by checking the label for 'Elrose Labs' and identifying if the product is still within its expiration date, as all unexpired batches are included in this recall.
  3. For Conzerol zero Topical Cream, verify the package shows NDC number 70223-001-06.
  4. Contact your healthcare provider or pharmacist for guidance on whether you should continue using these products.
  5. Return any unused product to the place of purchase for a full refund or contact the manufacturer, Elroselabs Inc., at 3875 Saint Johns Pkwy, Sanford, Florida, 32771-6371 for further instructions.
  6. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Healthcare provider consultation and pharmacy refund

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Conzerol zero molluscum contagiosum, Topical Cream (0.78 oz / 22g)
Model:
D-0621-2018
NDC 70223-001-06
Lot Numbers:
All product within expiry
Product: Molleave (2 oz bottle)
Model:
D-0622-2018
Lot Numbers:
All product within expiry
Product: Conzerol (antipoxin) H2O2 Gel, Hydrogen Peroxide Gel 3% (1.5 oz tube)
Model:
D-0623-2018
Lot Numbers:
All product within expiry

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 79606
Status: Resolved
Manufacturer: Elroselabs Inc.
Manufactured In: United States
Units Affected: 3 products (Unknown; Unknown; Unknown)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.