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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.

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Low RiskFDA Drug
Medications & Supplements/Over-the-Counter

The Mentholatum Company: Red Cross Oral Pain Blister Packs Recalled for Labeling Error

Agency Publication Date: August 24, 2020
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Summary

The Mentholatum Company has voluntarily recalled approximately 31,732 units of Red Cross Oral Pain (benzocaine 20%) maximum strength medication packaged in blister packs. This recall was initiated because the cotton pellet box included in the blister pack incorrectly states that the product contains "Natural Eugenol Oil," which it does not. Consumers should contact their healthcare provider or pharmacist regarding the use of this product and return any unused portions to the place of purchase for a refund.

Risk

The product is being recalled due to a labeling error regarding the ingredients; it does not contain Natural Eugenol Oil as stated on the internal cotton pellet box. While this is a low-risk labeling issue, inaccurate ingredient lists can lead to confusion or inappropriate treatment expectations for consumers.

What You Should Do

  1. Check your Red Cross Oral Pain (Oral Anesthetic benzocaine 20%) Maximum Strength blister pack (1/8 Fl. Oz. / 3.7 mL) for UPC 3 10742 09509 8 and NDC 10742-8902-1.
  2. Verify if your product belongs to Lot 66572 (Item Number 95090007), which is the specific lot affected by this labeling error.
  3. If your product is part of the recalled lot, contact your healthcare provider or pharmacist for guidance on its use.
  4. Return any unused product to the pharmacy or retail store where it was purchased for a full refund.
  5. Contact The Mentholatum Company at their headquarters in Orchard Park, NY for further instructions regarding this voluntary recall.
  6. For additional questions or to report a complaint, call 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

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

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

Affected Products

Product: Red Cross Oral Pain (Oral Anesthetic benzocaine 20%), Maximum Strength (1/8 Fl. Oz. / 3.7 mL)
Model:
NDC 10742-8902-1
Item Number: 95090007
UPC Codes:
310742095098
Lot Numbers:
66572

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 86154
Status: Resolved
Manufacturer: The Mentholatum Company
Manufactured In: United States
Units Affected: 31,732 Blister Packs
Distributed To: Nationwide

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.