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

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.

© 2026 Go Backs. All rights reserved.

Medium RiskFDA Drug
Medications & Supplements/Topical Products

Yusef Manufacturing Laboratories, LLC: Peppermint and Flavored Lip Moisturizers Recalled for Excessive Oxybenzone

Agency Publication Date: April 22, 2020
Share:
Sign in to monitor this recall

Summary

Yusef Manufacturing Laboratories has recalled 12,983 tubes of SPF 15 Peppermint, Flavored, and standard Lip Moisturizers because they contain up to 150% of the labeled amount of the active ingredient Oxybenzone. These products were distributed nationwide and sold under various brand names including Bimark, NOCO Trail Report, Herbruck's, and several dental or medical centers. Consumers should stop using the affected lip balms as they are superpotent and contain higher chemical levels than intended for sun protection.

Risk

The product is superpotent, containing significantly higher levels of the active sunscreen ingredient Oxybenzone than specified on the label, which may increase the risk of skin irritation or sensitivity.

What You Should Do

  1. Check your lip moisturizer tube to see if it is labeled as Peppermint Lip Moisturizer, Flavored Lip Moisturizer, or Lip Moisturizer with SPF 15.
  2. Locate the lot number on the tube packaging to see if it matches lot number 14381 with an expiration date of 9/2023.
  3. Confirm the brand or provider name on the label; affected tubes were distributed through various locations including Bimark Inc., NOCO TRAIL REPORT, St. Mark's Outpatient Surgery Center, Creekside Dental, Children's Healthcare of Atlanta, Great Smiles Orthodontics, and Gregory P. Miller DDS.
  4. Stop using the product immediately if it matches the affected lot number.
  5. Contact your healthcare provider or pharmacist for guidance regarding the use of this superpotent drug product.
  6. Return any unused product to the place of purchase for a refund and contact Yusef Manufacturing Laboratories for further instructions.
  7. 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

💰Full Refund

Contact healthcare provider and return product.

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

Affected Products

Product: PEPPERMINT LIP MOISTURIZER (oxybenzone 4% and Octinoxate 7%) SPF 15 (4.2 g tube)
Model:
D-1251-2020
Lot Numbers:
14381 (Exp. Date 9/2023)
Date Ranges: Expiration Date: 9/2023
Product: FLAVORED LIP MOISTURIZER (oxybenzone 4% and Octinoxate 7%) SPF 15 (4.2 g tube)
Model:
D-1251-2020
Lot Numbers:
14381 (Exp. Date 9/2023)
Date Ranges: Expiration Date: 9/2023
Product: LIP MOISTURIZER (oxybenzone 4% and Octinoxate 7%) SPF 15 (4.2 g tube)
Model:
D-1251-2020
Lot Numbers:
14381 (Exp. Date 9/2023)
Date Ranges: Expiration Date: 9/2023

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 85323
Status: Resolved
Manufacturer: Yusef Manufacturing Laboratories, LLC
Sold By: Bimark Inc.; NOCO TRAIL REPORT; Herbruck's; St. Mark's Outpatient Surgery Center; Trust Company Oklahoma; Creekside Dental; Children's Healthcare of Atlanta Hughes Spalding; Great Smiles Orthodontics; Acceleration station; The Children's Therapy & Learning Center; Gregory P. Miller DDS FAGD; Carolina Custom Traders; Palm Springs Dental Associates; Family Dental of Thronton
Manufactured In: United States
Units Affected: 12,983 tubes
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 · 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.