Yusef PEPPERMINT LIP MOISTURIZER Recall: High Oxybenzone Content Risk
Yusef Manufacturing Laboratories recalls PEPPERMINT LIP MOISTURIZER with high oxybenzone content (up to 150% of label) that may cause adverse reactions. Consumers should check product details and contact the manufacturer.
Stop using this now
Superpotent drug: This lot of SPF containing lip balm contains up to 150% of the label claim for active ingredient Oxybenzone.
Contact the company
What happened, in plain English
Yusef Manufacturing Laboratories is recalling their PEPPERMINT LIP MOISTURIZER due to potentially containing up to 150% of the labeled oxybenzone content. This high concentration could cause adverse reactions in some users, making it unsafe for normal use. Read more at govinfonow.com/recall/37348-yusef-peppermint-lip-moisturizer-recall-high-oxybenzone-content-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/37348-yusef-peppermint-lip-moisturizer-recall-high-oxybenzone-content-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-1251-2020
Cite this page
“Yusef PEPPERMINT LIP MOISTURIZER Recall: High Oxybenzone Content Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37348-yusef-peppermint-lip-moisturizer-recall-high-oxybenzone-content-risk. Based on FDA recall #D-1251-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1251-2020%22&limit=1).
Why it’s dangerous
The recalled lip balm contains up to 150% of the labeled amount of oxybenzone, a chemical that can cause skin irritation, allergic reactions, or other adverse effects when used in high concentrations. This exceeds the safe levels typically found in skincare products.
Who’s affected
People who own or use the recalled PEPPERMINT LIP MOISTURIZER (oxybenzone 4% and Octinoxate 7% SPF 15, 4.2g tube) are affected. Those with sensitive skin or allergies to oxybenzone are at higher risk.
How to tell if you have this one
Check for the product labeled as PEPPERMINT LIP MOISTURIZER with oxybenzone (4%) and Octinoxate (7%) SPF 15, 4.2g tube. The recall includes specific retailers and lot number 14381 (expires 9/2023).
- Brand
Yusef Manufacturing Laboratories- Category
Drug
What to do — step by step
Stop Using Now
Immediately stop using the recalled lip balm as it contains up to 150% of the labeled oxybenzone content, which may cause adverse reactions.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide within the United States” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 3.9 years after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Where can I find the product?
The product was sold at specific retailers including Bimark Inc., Herbruck's, St. Mark's Outpatient Surgery Center, and others listed in the recall notice.
Contact Yusef Manufacturing Laboratories
We’ve drafted a message you can send Yusef Manufacturing Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-1251-2020 — Yusef Manufacturing Laboratories Yusef PEPPERMINT LIP MOISTURIZER Recall: High Oxybenzone Content R Hello, I own a Yusef PEPPERMINT LIP MOISTURIZER Recall: High Oxybenzone Content Risk that is covered by recall D-1251-2020 from Yusef Manufacturing Laboratories. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1251-2020 (March 3, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1251-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.