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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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High RiskFDA Drug
Medications & Supplements/Topical Products

Lotrimin and Tinactin Spray Products Recalled for Benzene Contamination

Agency Publication Date: November 18, 2021
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Summary

Bayer Healthcare Pharmaceuticals Inc. is recalling more than 44,302,392 cans of Lotrimin AF and Tinactin aerosol spray products, including deodorant powder, jock itch, and liquid sprays. This recall was initiated after some products were found to contain benzene, a known human carcinogen, or were manufactured at a facility with existing contamination issues. No injuries or illnesses have been reported. These products were sold nationwide through retail stores and online channels across the United States, Puerto Rico, Canada, and Mexico.

Risk

Benzene is classified as a human carcinogen, and exposure can occur through inhalation, orally, and through the skin. Long-term exposure to benzene can potentially lead to life-threatening cancers, such as leukemia, and other blood disorders.

What You Should Do

  1. This recall involves multiple varieties of Lotrimin AF and Tinactin aerosol spray products, including Deodorant Powder Spray, Jock Itch Powder Spray, Liquid Spray, and Daily Prevention sprays sold in 4.6 oz, 5.3 oz, and 5.6 oz cans.
  2. Check the bottom of your spray can for the lot number and compare it with the affected list. See the Affected Products section below for the full list of affected codes.
  3. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for more information.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: LOTRIMIN AF Deodorant Powder Spray (133g/4.6 oz)
Variants: Miconazole nitrate 2%, Product of Spain
UPC Codes:
311017410233
Lot Numbers:
TN00082 (Exp 9/30/2021)
TN000TU (Exp 10/31/2021)
TN000TV (Exp 10/31/2021)
TN00236 (Exp 1/31/2022)
TN003C8 (Exp 2/28/2022)
TN003C9 (Exp 3/31/2022)
TN003GS (Exp 4/30/2022)
TN0041W (Exp 6/30/2022)
TN006W8 (Exp 8/31/2022)
TN005P5 (Exp 9/30/2022)
TN006MZ (Exp 2/28/2023)
TN008D3 (Exp 5/31/2023)
TN009K7 (Exp 5/31/2023)
NDC:
11523-1272-2

Recalled under identifiers D-0236-2022 and D-0246-2022.

Product: LOTRIMIN AF Jock Itch Powder Spray (133g/4.6 oz)
Variants: Miconazole nitrate 2%, Product of Spain
UPC Codes:
311017410318
Lot Numbers:
CV01BEP (Exp 3/31/2022)
CV01D6W (Exp 5/31/2022)
CV01EV0 (Exp 7/31/2022)
TN0004J (Exp 9/30/2022)
TN001AE (Exp 11/30/2022)
TN003C3 (Exp 1/31/2023)
TN003C4 (Exp 2/28/2023)
TN003HT (Exp 3/31/2023)
TN003CW (Exp 4/30/2023)
TN0045J (Exp 6/30/2023)
TN0040C (Exp 7/31/2023)
TN004BU (Exp 8/31/2023)
TN006MB (Exp 9/30/2022)
CV018TV (Exp 11/30/2021)
CV01A71 (Exp 1/31/2022)
CV01CK4 (Exp 4/30/2022)
TN0023G (Exp 12/31/2022)
TN006TC (Exp 1/31/2023)
TN007TG (Exp 3/31/2023)
TN008CZ (Exp 4/30/2023)
TN008CY (Exp 4/30/2023)
NDC:
11523-4140-2

Recalled under identifiers D-0237-2022 and D-0247-2022.

Product: Tinactin Deodorant Powder Spray (133g/4.6 oz)
Variants: Tolnaftate 1%, Product of Finland
Model:
20006105
86568411
UPC Codes:
311017410004
Lot Numbers:
TN0067A (Exp 2/28/2023)
TN008CU (Exp 4/30/2023)
TN004BW (Exp 7/31/2022)
TN00678 (Exp 8/31/2022)
TN00679 (Exp 9/30/2022)
NDC:
11523-4162-1

Recalled under identifiers D-0250-2022 and D-0242-2022.

Product: Tinactin Liquid Spray (150g/5.3 oz)
Variants: Tolnaftate 1%, Product of Finland, Product of Ireland
Model:
20006101
87022897
UPC Codes:
311017410059
Lot Numbers (59):
TN006MX (Exp 10/31/2022)
TN00BKV (Exp 3/31/2023)
TN008D1 (Exp 3/31/2023)
TN008D2 (Exp 3/31/2023)
CV0180B (Exp 12/31/2021)
TN003C5 (Exp 1/31/2023)
TN0060U (Exp 7/31/2022)
TN0060V (Exp 7/31/2022)
TN0060W (Exp 7/31/2022)
TN0060X (Exp 9/30/2022)
TN0060Y (Exp 9/30/2022)
TN0060Z (Exp 9/30/2022)
TN006CJ (Exp 9/30/2022)
TN006CK (Exp 9/30/2022)
TN006CM (Exp 9/30/2022)
TN00610 (Exp 9/30/2022)
TN006YW (Exp 10/31/2022)
TN006MY (Exp 12/31/2022)
TN006YX (Exp 12/31/2022)
TN006YY (Exp 12/31/2022)
TN007EN (Exp 2/28/2023)
TN007EP (Exp 2/28/2023)
TN007ER (Exp 2/28/2023)
CV016TH (Exp 10/31/2021)
CV016TJ (Exp 10/31/2021)
CV017D8 (Exp 10/31/2021)
CV017D7 (Exp 10/31/2021)
CV017XS (Exp 11/30/2021)
CV01980 (Exp 12/31/2021)
CV019DS (Exp 12/31/2021)
CV01A72 (Exp 1/31/2022)
CV01A73 (Exp 1/31/2022)
CV01AE6 (Exp 1/31/2022)
CV01AUA (Exp 2/28/2022)
CV01B1E (Exp 2/28/2022)
CV01BNE (Exp 3/31/2022)
CV01BVU (Exp 3/31/2022)
CV01CT6 (Exp 4/30/2022)
CV01CY1 (Exp 4/30/2022)
CV01D2G (Exp 5/31/2022)
CV01DRX (Exp 6/30/2022)
CV01DRY (Exp 6/30/2022)
CV01E2T (Exp 6/30/2022)
CV01E2W (Exp 7/31/2022)
CV01E2X (Exp 7/31/2022)
CV01E2U (Exp 7/31/2022)
CV01E2V (Exp 8/31/2022)
TN001V6 (Exp 11/30/2022)
TN00243 (Exp 12/31/2022)
TN0024B (Exp 1/31/2023)
NDC:
11523-0165-3

Recalled under identifiers D-0251-2022 and D-0243-2022.

Product: Tinactin Jock Itch Powder Spray (133g/4.6 oz)
Variants: Tolnaftate 1%, Product of Finland, Product of Ireland
Model:
20066104
86951967
UPC Codes:
311017410073
Lot Numbers:
TN008M0 (Exp 4/30/2023)
TN00086 (Exp 10/31/2022)
CV015YU (Exp 10/31/2022)
TN00273 (Exp 12/31/2022)
TN005RW (Exp 5/31/2023)
NDC:
11523-0072-5

Recalled under identifiers D-0252-2022 and D-0244-2022.

Product: Tinactin Powder Spray (133g/4.6 oz)
Variants: Tolnaftate 1%, Product of Finland, Product of Ireland
Model:
20006106
86940418
UPC Codes:
311017410097
Lot Numbers:
CV015YS (Exp 9/30/2021)
TN008CT (Exp 3/31/2023)
TN007TJ (Exp 3/31/2023)
CV015YT (Exp 10/31/2021)
CV01AE7 (Exp 2/28/2022)
CV01CY2 (Exp 4/30/2022)
CV01E6P (Exp 8/31/2022)
TN00085 (Exp 10/31/2022)
TN001EK (Exp 10/31/2022)
TN001ZV (Exp 12/31/2022)
TN00274 (Exp 12/31/2022)
TN003CU (Exp 1/31/2023)
TN003CV (Exp 3/31/2023)
TN0047H (Exp 4/30/2023)
TN0047R (Exp 5/31/2023)
TN0067B (Exp 9/30/2022)
TN006AT (Exp 12/31/2022)
TN006TA (Exp 2/28/2023)
CV01E6PV (Exp 8/31/2022)
CV01E6PD (Exp 8/31/2022)
CV01E6PC (Exp 8/31/2022)
CV01E6PBV (Exp 8/31/2022)
CV01E6PAV (Exp 8/31/2022)
NDC:
11523-0777-2

Recalled under identifiers D-0253-2022 and D-0245-2022.

Product: LOTRIMIN AF Daily Prevention Deodorant Powder Spray (160g/5.6 oz)
Variants: Tolnaftate 1%, Product of Finland
UPC Codes:
041100587206
041100589613
00041100590756
Lot Numbers:
NAA8997 (Exp 01/31/2022)
NAA8EK8 (Exp 02/28/2022)
NAA9E18 (Exp 08/31/2022)
NAA9LFP (Exp 08/31/2022)
NAA9T53 (Exp 08/31/2022)
NAA5RW (Exp 08/31/2022)
TN0023C (Exp 1/31/2022)
TN003C7 (Exp 4/30/2022)
TN00570 (Exp 7/31/2022)
TN0056Z (Exp 8/31/2022)
TN005KJ (Exp 8/31/2022)
TN0023DV (Exp 2/28/2022)
TN0023DAV (Exp 2/28/2022)
TN0023DBV (Exp 2/28/2022)
TN0023DC (Exp 2/28/2022)
TN005KJA (Exp 08/31/2022)
TN005KJB (Exp 08/31/2022)
TN0023D (Exp 2/28/2022)
TN004BX (Exp 6/30/2022)
NDC:
11523-0010-2

Includes ECOM PK varieties and sets with Lotrimin Ultra cream. Recalled under D-0254-2022, D-0240-2022, and D-0249-2022.

Product: LOTRIMIN AF Powder Spray (133g/4.6 oz)
Variants: Miconazole nitrate 2%, Product of Spain
UPC Codes:
311017410257
041100585943
Lot Numbers:
CV017D9 (Exp 10/31/2021)
CV01940 (Exp 11/30/2021)
CV01CD9 (Exp 4/30/2022)
CV01D9T (Exp 6/30/2022)
CV01DZ3 (Exp 6/30/2022)
CV01EPP (Exp 7/31/2022)
TN000TT (Exp 10/31/2022)
TN003CG (Exp 1/31/2023)
TN003CH (Exp 3/31/2023)
TN00407 (Exp 3/31/2023)
TN0041V (Exp 6/30/2023)
TN0056W (Exp 7/31/2022)
TN005P4 (Exp 8/31/2022)
TN006MJ (Exp 9/30/2022)
CV01940A (Exp 11/30/2021)
CV01AP2 (Exp 02/28/2022)
CV01D9TA (Exp 06/30/2022)
TN000TTA (Exp 10/31/2022)
TN003CHA (Exp 03/31/2023)
TN006TD (Exp 3/31/2023)
TN006TDB (Exp 03/31/2023)
TN00407A (Exp 03/31/2023)
TN008CV (Exp 4/30/2023)
TN008CW (Exp 5/31/2023)
NDC:
11523-0544-2

Recalled under identifiers D-0238-2022 and D-0248-2022.

Product: LOTRIMIN AF Daily Prevention Deodorant Powder Spray (133g/4.6 oz)
Variants: Tolnaftate 1%, Product of Finland
UPC Codes:
041100590367
Lot Numbers:
TN005K4 (Exp 4/30/2022)
TN005K8 (Exp 6/30/2022)
NDC:
11523-0010-1

Recalled under identifier D-0239-2022.

Product: Lotrimin AF Liquid Spray (133g/4.6 oz)
Variants: Miconazole nitrate 2%, Product of Spain
UPC Codes:
041100407887
041100585936
Lot Numbers:
TN000TR (Exp 10/31/2021)
TN0011B (Exp 11/30/2021)
TN003CC (Exp 2/28/2022)
TN003CD (Exp 2/28/2022)
TN0040B (Exp 5/31/2022)
TN0041U (Exp 6/30/2022)
TN004BK (Exp 8/31/2022)
TN005P3 (Exp 10/31/2022)
TN006AP (Exp 1/31/2023)
TN006MC (Exp 1/31/2023)
TN006TB (Exp 4/30/2023)
TN0011BA (Exp 11/30/2021)
TN003CDA (Exp 02/28/2022)
TN003CDB (Exp 02/28/2022)
TN0040BA (Exp 05/31/2022)
TN0040BV (Exp 05/31/2022)
NDC:
11523-4327-1

Recalled under identifier D-0241-2022.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 88677
Status: Resolved
Manufacturer: Bayer Healthcare Pharmaceuticals Inc.
Sold By: retail channels
Manufactured In: United States, Spain, Finland, Ireland, Japan
Units Affected: 19 products (2,817,468 cans; 4,546,152 cans; 3,816,468 cans; 77,076 cans; 579,456 cans; 1,801,332 cans; 738,432 cans; 4,990,860 cans; 592,416 cans; 2,841,012 cans; 2,817,468 cans; 4,546,152 cans; 3,816,468 cans; 579,456 cans; 738,432 cans; 4,990,860 cans; 592,416 cans; 2,841,012 cans; 579,456 units)
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.

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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 FDA Press Release 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.