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Benzoyl Peroxide Benzene Tracker

Search every benzoyl peroxide acne product named in the 2025 FDA-announced benzene recalls, a Health Canada recall and independent lab testing, by brand, product or lot number. Each entry links to its source.

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Short version: the FDA tested 95 benzoyl peroxide products and found undetectable or very low benzene in more than 90% of them. Specific lots of seven products were recalled from store shelves. If your lot number isn't on the list, there is no recall for it. Either way, keeping benzoyl peroxide cool and replacing it regularly limits benzene formation. For the background, read our guide to benzene in benzoyl peroxide.

95

benzoyl peroxide products tested by the FDA (announced March 11, 2025)

7

US products with recalled lots after benzene findings

1

Health Canada recall covering multiple Proactiv lots

65

recalled lot numbers you can search below

Data last checked . Next scheduled audit by . How we build and check this list.

Showing all 13 entries.

Benzoyl peroxide products named in benzene recalls or independent benzene testing, with lot numbers and sources
Product Status Lot numbers (expiration) What happened Source
La Roche-Posay Effaclar Duo Dual Action Acne Treatment Treatment (leave-on) · US Recalled Retail recall Finding: FDA testing
  • MYX46W exp. April 2025

One lot voluntarily recalled at the retail level after FDA testing found elevated benzene. Stores were told to remove it from shelves and online listings.

Only lot MYX46W was named. Other lots of this product were not part of the recall.

U.S. Food and Drug Administration Published Also reported by: ABC News, NPR Last checked Not yet confirmed against the primary source
Proactiv Emergency Blemish Relief Cream Benzoyl Peroxide 5% BPO 5% · Spot treatment (leave-on) · US Recalled Retail recall Finding: FDA testing
  • V3305A exp. October 2025
  • V3304A exp. October 2025

Two lots voluntarily recalled at the retail level after the FDA shared its benzene test results with the maker, Alchemee. News reports of the FDA enforcement entry describe it as a Class II recall.

U.S. Food and Drug Administration Published Also reported by: The Healthy (Trusted Media Brands), Newsweek Last checked Not yet confirmed against the primary source
Proactiv Proactiv and Proactiv+ products with 2.5% or 5% benzoyl peroxide (several products and sets) BPO 2.5% or 5% · Several (cleansers, treatments, exfoliators, sets) · Canada Recalled Finding: Health Canada recall notice
35 lot numbers
  • T4066A
  • T4221A
  • T3244A
  • T4047A
  • T4047B
  • T4051A
  • T3352A
  • T3353A
  • T4046A
  • T4226A
  • V4330A
  • V4355A
  • V4281A
  • V4066A
  • V4068A
  • V4067A
  • V4068B
  • SC5029A
  • SC5029B
  • SC5028A
  • V4050A
  • V4051A
  • V4204A
  • V4205A
  • V4040A
  • V4043B
  • V4044B
  • V4277A
  • V4277C
  • SC5013A
  • V4235A
  • SC4333A
  • SC4332A
  • SC4130A
  • V4234A

Expiration dates not confirmed.

Health Canada posted a recall of specific lots of Proactiv and Proactiv+ benzoyl peroxide products sold in Canada because benzene in those lots may be outside the allowable limit. Its advice to consumers is to check whether a product is affected, stop using it, and talk to a health care professional about any concerns.

This is a Canadian recall and covers Canadian lots. The Health Canada notice lists each product and its Drug Identification Number (DIN). We could not confirm the notice's publication date, so it is left blank. Check the notice for the full product list. We have not confirmed the recall classification on the notice, so it is not shown.

Health Canada Publication date not confirmed Also reported by: OurWindsor.ca Last checked Not yet confirmed against the primary source
Proactiv Skin Smoothing Exfoliator Exfoliating cleanser (wash-off) · US Recalled Retail recall Finding: FDA testing
  • V4204A exp. July 2025

One lot voluntarily recalled at the retail level after FDA testing found elevated benzene. News reports of the FDA enforcement entry describe it as a Class II recall.

Most reports give the lot as V4204A. At least one secondary report printed V4202A, which we believe is a typo. Check the FDA page if your lot is close to either.

U.S. Food and Drug Administration Published Also reported by: The Healthy (Trusted Media Brands), Health Canada Last checked Not yet confirmed against the primary source
SLMD Skincare Benzoyl Peroxide Acne Lotion Lotion (leave-on) · US Recalled Retail recall Finding: FDA testing
  • 2430600 exp. March 2025

One lot voluntarily recalled at the retail level after FDA testing found elevated benzene. This lot's expiration date has passed, so it should be thrown away anyway.

U.S. Food and Drug Administration Published Also reported by: LAist Last checked Not yet confirmed against the primary source
Walgreens Acne Control Cleanser Cleanser (wash-off) · US Recalled Retail recall Finding: FDA testing
  • 23 09328 exp. September 2025

One lot voluntarily recalled at the retail level after FDA testing found elevated benzene.

The lot number is printed with a space ("23 09328"). Search works with or without the space.

U.S. Food and Drug Administration Published Also reported by: Newsweek, LAist Last checked Not yet confirmed against the primary source
Walgreens Tinted Acne Treatment Cream Tinted cream (leave-on) · US Recalled Retail recall Finding: FDA testing
  • 49707430 exp. March 2026

One lot voluntarily recalled at the retail level after FDA testing found elevated benzene.

U.S. Food and Drug Administration Published Also reported by: LAist, Newsweek Last checked Not yet confirmed against the primary source
Zapzyt Acne Treatment Gel 10% Benzoyl Peroxide BPO 10% · Gel (leave-on) · US Recalled Retail recall Finding: Manufacturer's own testing
23 lot numbers
  • 0153
  • 0154
  • 0155
  • 0156
  • 0161
  • 0326
  • 0327
  • 0328
  • 0329
  • 0479
  • 0480
  • 9762
  • 9763
  • 9764
  • 9765
  • 9869
  • 9870
  • 9871
  • 9872
  • 9995
  • 9996
  • 9997
  • 9998

Expiration dates not confirmed.

Voluntarily recalled at the retail level after the manufacturer's own testing found elevated benzene. The FDA listed it alongside the six products from its own testing. Reports of the FDA enforcement entry name Denison Pharmaceuticals, LLC as the recalling firm.

The lot list comes from a retailer recall notice and news reports of the FDA enforcement entry. We could not confirm expiration dates for these lots, so they are left blank rather than guessed.

U.S. Food and Drug Administration Published Also reported by: Dierbergs Markets (retailer recall notice), The Healthy (Trusted Media Brands) Last checked Not yet confirmed against the primary source
Clearasil (Reckitt) Clearasil 10% benzoyl peroxide cream (as identified in the petition) BPO 10% · Cream (leave-on) · US Independent testing Finding: Valisure (independent lab), heat-stress testing No lots named

Named in Valisure's March 2024 citizen petition. Media coverage reported benzene at 308 ppm after heat incubation in the lab.

Reported benzene: 308 ppm (after heat incubation, as reported)

Not part of the FDA's March 2025 recall list. Being named here does not mean the FDA recalled this product or found it unsafe. The figure comes from news coverage of the petition; we have not yet matched it, the exact product name and the test conditions to the petition document itself.

CBS News (reporting Valisure's citizen petition) Published Also reported by: Valisure, LLC (petition PDF) Last checked Not yet confirmed against the primary source
Clinique (Estée Lauder) Clinique 2.5% benzoyl peroxide cream (as identified in the petition) BPO 2.5% · Cream (leave-on) · US Independent testing Finding: Valisure (independent lab), heat-stress testing No lots named

Named in Valisure's March 2024 citizen petition. Media coverage reported benzene at 401 ppm after heat incubation in the lab.

Reported benzene: 401 ppm (after heat incubation, as reported)

Not part of the FDA's March 2025 recall list. Being named here does not mean the FDA recalled this product or found it unsafe. The figure comes from news coverage of the petition; we have not yet matched it, the exact product name and the test conditions to the petition document itself.

CBS News (reporting Valisure's citizen petition) Published Also reported by: Valisure, LLC (petition PDF) Last checked Not yet confirmed against the primary source
Proactiv Proactiv 2.5% benzoyl peroxide cream (as identified in the petition) BPO 2.5% · Cream (leave-on) · US Independent testing Finding: Valisure (independent lab), heat-stress testing No lots named

Named in Valisure's March 2024 citizen petition to the FDA. Media coverage of the petition reported benzene at 1,761 ppm, measured after the lab incubated the product at elevated temperature. That is not the same as measuring the product as sold.

Reported benzene: 1,761 ppm (after heat incubation, as reported)

The FDA's own 2025 testing did not confirm widespread contamination. Being named here does not mean the FDA recalled this product or found it unsafe. The figure comes from news coverage of the petition; we have not yet matched it, the exact product name and the test conditions to the petition document itself.

CBS News (reporting Valisure's citizen petition) Published Also reported by: Valisure, LLC (petition PDF) Last checked Not yet confirmed against the primary source
Target (Up & Up) Up & Up 2.5% benzoyl peroxide cream (as identified in the petition) BPO 2.5% · Cream (leave-on) · US Independent testing Finding: Valisure (independent lab), heat-stress testing No lots named

Named in Valisure's March 2024 citizen petition. Media coverage reported benzene at 1,598 ppm after heat incubation in the lab.

Reported benzene: 1,598 ppm (after heat incubation, as reported)

Not part of the FDA's March 2025 recall list. Being named here does not mean the FDA recalled this product or found it unsafe. The figure comes from news coverage of the petition; we have not yet matched it, the exact product name and the test conditions to the petition document itself.

CBS News (reporting Valisure's citizen petition) Published Also reported by: Valisure, LLC (petition PDF) Last checked Not yet confirmed against the primary source
Walgreens Walgreens 10% benzoyl peroxide cream (as identified in the petition) BPO 10% · Cream (leave-on) · US Independent testing Finding: Valisure (independent lab), heat-stress testing No lots named

Named in Valisure's March 2024 citizen petition. Media coverage reported benzene at 114 ppm after heat incubation in the lab. This is a different product from the two Walgreens products recalled in 2025.

Reported benzene: 114 ppm (after heat incubation, as reported)

Being named here does not mean the FDA recalled this product or found it unsafe. The figure comes from news coverage of the petition; we have not yet matched it, the exact product name and the test conditions to the petition document itself.

CBS News (reporting Valisure's citizen petition) Published Also reported by: Valisure, LLC (petition PDF) Last checked Not yet confirmed against the primary source

What each status means

Recalled
Specific lots were voluntarily recalled after benzene findings (announced by the FDA, or by Health Canada for Canadian lots).
Independent testing
Named in an independent lab's findings (Valisure's 2024 FDA citizen petition), often after heat-stress testing. Not an FDA finding and not a recall.
Low / not detected
Named by the FDA as tested with benzene undetectable or extremely low. (No product-level FDA results have been published yet.) No entries yet.

As of our last check, the FDA had published the names of the recalled products only, not product-by-product results for the other products it tested. That is why this tracker has no 'tested below threshold' rows yet. If the FDA publishes full results, we will add them.

Download the data: JSON CSV Data licensed under CC BY 4.0: free to reuse with credit to AcneRid and a link to this page.

How to check your product in under a minute

  1. Find the lot number and expiration date. Look for "LOT" and "EXP" stamped on the crimped end of a tube, the bottom of a bottle or pump, or the carton. They're often printed in small, low-contrast type.
  2. Type the lot number into the search box above. Spaces and dashes don't matter, so 2309328 finds lot 23 09328.
  3. Check that the product matches. A lot match only counts if the brand and product name on your package match the entry too.
  4. No match? Then no recall we know of covers your lot. Throw the product out if it's past its expiration date, and follow the storage tips below.

Our step-by-step guide, how to find the lot number on benzoyl peroxide, walks through reading lot codes, asking for a refund and what to do next.

What to do if your product was recalled

The 2025 U.S. recalls were retail-level recalls. The FDA told stores to take the named lots off shelves and online listings. It did not tell people to take any particular action with products they already owned, apart from throwing away expired ones. The FDA also said that even with daily use for decades, the risk of developing cancer from the benzene found in these products is very low.

That said, most people prefer not to keep using a recalled lot. Reasonable steps:

  • Stop using that tube or bottle. Switching to another product with the same active ingredient and strength usually lets you continue your routine without a break.
  • Ask about a refund or replacement. Contact the retailer or the manufacturer's customer service, and have the lot number and a photo of the label ready. News reports said Proactiv's maker offered refunds or replacements for its recalled lots.
  • Dispose of it sensibly. The FDA's general advice for medicines without a take-back option is to mix them with something unappealing, such as used coffee grounds, seal the mixture in a bag and put it in household trash. See the FDA's medicine disposal guidance.
  • In Canada, Health Canada's advice for the recalled Proactiv lots is to check whether your product is affected, stop using it, and talk to a health care professional if you have concerns.
  • Report a reaction. If you had a side effect from any acne product, you can report it to the FDA through MedWatch.

How to store benzoyl peroxide to limit benzene

Benzoyl peroxide is chemically unstable, and heat speeds up its breakdown into benzene. In a 2024 study in Environmental Health Perspectives, benzene rose in products kept at body temperature (37°C/98.6°F) for several weeks, and much more at 50°C (122°F) and 70°C (158°F). A 2025 study in the Journal of Investigative Dermatology found benzene could form at room temperature too, and that cold storage greatly reduced it. The American Academy of Dermatology suggests:

  • Store products as the label directs, generally at room temperature or cooler. A refrigerator is fine.
  • Replace benzoyl peroxide products about every 10 to 12 weeks.
  • Throw out products that have been exposed to higher temperatures (for example, above 78°F).

Practical ways to do that:

  • Don't leave acne products in a car, a gym bag in the sun, or on a sunny windowsill.
  • Keep a leave-on product out of a hot, steamy shower caddy if you can.
  • Buy the size you'll finish in a couple of months rather than a jumbo tube that sits open for a year.
  • Check the expiration date when you buy, and again before each new tube goes into use.

How we build and check this list

What's included

  • Recalled: products and lot numbers named in the FDA's March 11, 2025 announcement, and lots named in a Health Canada recall notice.
  • Named in independent testing: products named, with reported benzene levels where we could confirm them, in coverage of Valisure's March 2024 citizen petition to the FDA. These are not FDA findings and not recalls.
  • FDA tested, low or not detected: reserved for products the FDA names as tested with low or undetectable benzene. As of our last check, the FDA had published the names of the recalled products only, not product-by-product results for the other products it tested. That is why this tracker has no 'tested below threshold' rows yet. If the FDA publishes full results, we will add them.

How each entry is sourced

Every row lists its primary source (the FDA, Health Canada or the petition), the date the finding was announced, the other reports we checked it against, and the date we last checked it. Recall rows reproduce the FDA's March 11, 2025 recall table as reported by several independent outlets and retailer notices, plus a Health Canada recall notice. Independent-testing rows come from news coverage of Valisure's March 2024 citizen petition and list only products that coverage tied to a specific benzene figure; brands named without a specific product and figure are not listed. Each row lists its primary source and the secondary reports we checked it against. Rows marked 'Checked against secondary reports' should be re-checked against the primary page at the next audit. We don't do any laboratory testing ourselves, and we don't guess at missing details. Where an expiration date or publication date couldn't be confirmed, the cell says so.

What the benzene numbers mean

FDA guidance, consistent with ICH Q3C, says benzene should be avoided in drug manufacturing and, where its use is unavoidable, kept below 2 parts per million (ppm) in drug products. Independent lab figures in this table were mostly measured after the products were heated on purpose, so they show what can form under heat stress, not what was in a typical tube on a store shelf.

How often we update it

We check for new FDA, Health Canada and manufacturer announcements at least once a quarter and whenever a new recall is reported. The data was last checked on . If you spot an error or a missing recall, please tell us through our corrections page; we log every correction publicly. Our editorial policy explains how we choose and check sources.

Why the FDA and Valisure results look so different

Valisure, an independent lab, told the FDA in March 2024 that it had found high benzene levels in many benzoyl peroxide products, with the highest figures after heating samples. The FDA then ran its own tests on 95 products, including the products third-party labs had flagged that it was able to buy. It found undetectable or extremely low benzene in more than 90% of them. The two sets of results measure different things. One shows what heat and time can do, and the other shows what was in products bought off the shelf at one point in time. A 2025 analysis in JAMA Dermatology of 111 products found that formulation mattered. Products with the antioxidant butylated hydroxytoluene (BHT) tended to have less benzene, and leave-on products had less than washes. The benzoyl peroxide percentage itself was not significantly linked to benzene levels.

What the health research says so far

Benzene is a known human carcinogen, so any exposure is worth minimizing. The studies so far on people who actually use benzoyl peroxide are reassuring. An analysis of U.S. national survey data (NHANES) found no link between benzoyl peroxide use and higher blood benzene levels. A large U.S. health-records study found no increase in cancers among people treated with benzoyl peroxide for acne. These are observational studies, so they can't rule out a very small risk, but they fit with the FDA's view that the risk is very low.

Benzoyl peroxide remains one of the best-supported acne treatments. The American Academy of Dermatology's 2024 guidelines strongly recommend it. If you'd like to avoid it anyway, read about choosing the right benzoyl peroxide strength, or use our acne treatment path quiz to see other options. To check a routine for ingredient clashes, try the ingredient conflict checker.

Frequently asked questions

Which benzoyl peroxide products were recalled for benzene?

On March 11, 2025 the FDA announced that specific lots of seven acne products were voluntarily recalled at the retail level: La Roche-Posay Effaclar Duo Dual Action Acne Treatment, Walgreens Acne Control Cleanser, Proactiv Emergency Blemish Relief Cream (5%), Proactiv Skin Smoothing Exfoliator, SLMD Benzoyl Peroxide Acne Lotion, Walgreens Tinted Acne Treatment Cream, and Zapzyt Acne Treatment Gel. Only the listed lots were recalled, not every tube of those products. Health Canada separately recalled specific lots of Proactiv and Proactiv+ products sold in Canada.

Should I stop using benzoyl peroxide because of benzene?

Not necessarily. The FDA found undetectable or extremely low benzene in more than 90% of the 95 products it tested, and it said that even with daily use for decades, the cancer risk from benzene in the recalled products is very low. The American Academy of Dermatology says there is no clear evidence that benzoyl peroxide acne products contain dangerous levels of benzene. If you would rather avoid it, a dermatologist can suggest alternatives such as a topical retinoid, salicylic acid or azelaic acid.

How do I check whether my product is part of the recall?

Find the lot number (often labeled LOT) and expiration date (EXP) on the tube crimp, the bottom of the bottle or the carton. Type the lot number into the search box on this page. A match means that lot was named in a recall. Also confirm that the product name matches, because unrelated products can share similar lot codes.

Why did Valisure report much higher benzene levels than the FDA?

Valisure's highest numbers came from products it deliberately heated in the lab, at temperatures such as 50°C (122°F) and 70°C (158°F), to show how benzene forms under heat stress. The FDA measured products as purchased, using validated methods. Both approaches tell you something: heat and time can increase benzene in some formulations, but most products tested as sold had very low levels.

My product is not on this list. Does that mean it tested clean?

No. The FDA has published the names of recalled products but not product-by-product results for everything it tested, and many products on the market were never tested. Not being listed means only that we have not found a recall or published test result naming it. Storing the product in a cool place and replacing it regularly reduces benzene formation regardless.

What should I do if I used a recalled product?

The FDA described the cancer risk from these products as very low, even with long-term daily use, and it did not ask consumers to take specific action because these were retail-level recalls. You can stop using the product, contact the retailer or manufacturer about a refund, and throw away anything past its expiration date. If you have health concerns, talk with a doctor or pharmacist.

Sources 14

  1. Limited number of voluntary recalls initiated after FDA testing of acne products for benzene; findings show a small number of products with elevated levels of benzene contamination (opens in a new tab) U.S. Food and Drug Administration , 2025
  2. FDA alerts drug manufacturers to the risk of benzene contamination in certain drugs (opens in a new tab) U.S. Food and Drug Administration
  3. Proactiv / Proactiv + BPO Products: Benzene Concentration Outside Allowable Limit (opens in a new tab) Health Canada
  4. Citizen Petition on Benzene in Benzoyl Peroxide Drug Products (opens in a new tab) Valisure, LLC , 2024
  5. Benzoyl Peroxide Drug Products Form Benzene (Kucera et al.) (opens in a new tab) Environmental Health Perspectives , 2024
  6. Evaluation of Benzene Presence and Formation in Benzoyl Peroxide Drug Products (opens in a new tab) Journal of Investigative Dermatology , 2025
  7. The Role of Formulation in Benzene Formation in Benzoyl Peroxide Products (opens in a new tab) JAMA Dermatology , 2025
  8. No evidence for an association between benzoyl peroxide use and increased blood benzene levels in the National Health and Nutrition Examination Survey (opens in a new tab) Journal of the American Academy of Dermatology , 2024
  9. Benzoyl peroxide for acne treatment is not associated with an increased risk of malignancy: A retrospective cohort study (opens in a new tab) Journal of the American Academy of Dermatology , 2024
  10. Guidelines of care for the management of acne vulgaris (Reynolds RV, et al.) (opens in a new tab) Journal of the American Academy of Dermatology , 2024
  11. FAQs: Benzene in acne products containing benzoyl peroxide (opens in a new tab) American Academy of Dermatology
  12. FDA Drug Safety Communication: FDA warns of rare but serious hypersensitivity reactions with certain over-the-counter topical acne products (opens in a new tab) U.S. Food and Drug Administration , 2014
  13. Disposal of Unused Medicines: What You Should Know (opens in a new tab) U.S. Food and Drug Administration
  14. MedWatch: The FDA Safety Information and Adverse Event Reporting Program (opens in a new tab) U.S. Food and Drug Administration

Medical review pending. This page was researched and written by the AcneRid Editorial Team from the cited sources, but it has not yet been reviewed by a licensed clinician. We update this notice when a review is complete. About our review process.