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<\/figure><\/li><\/ul><\/figure>\n\n\n\nThe affected Lotrimin\u00ae and Tinactin\u00ae spray products are over the counter antifungal products, sold individually or in combo packs. The impacted products are:<\/p>\n\n\n\n
- Lotrimin\u00ae Anti-Fungal (AF) Athlete’s Foot Powder Spray<\/li>
- Lotrimin\u00ae Anti-Fungal Jock Itch (AFJI) Athlete’s Foot Powder Spray<\/li>
- Lotrimin\u00ae Anti-Fungal (AF) Athlete\u2019s Foot Deodorant Powder Spray<\/li>
- Lotrimin\u00ae AF Athlete’s Foot Liquid Spray<\/li>
- Lotrimin\u00ae AF Athlete\u2019s Foot Daily Prevention Deodorant Powder Spray<\/li>
- Tinactin\u00ae Jock Itch (JI) Powder Spray<\/li>
- Tinactin\u00ae Athlete\u2019s Foot Deodorant Powder Spray<\/li>
- Tinactin\u00ae Athlete\u2019s Foot Powder Spray<\/li>
- Tinactin\u00ae Athlete\u2019s Foot Liquid Spray<\/li><\/ul>\n\n\n\n
Product images and information on which lot numbers fall under this recall are available at: https:\/\/livewell.bayer.com\/document\/2011<\/a>External Link Disclaimer<\/a>.<\/a>External Link Disclaimer<\/a><\/p>\n\n\n\n
There are no issues of concern with Lotrimin\u00ae\/Tinactin\u00ae creams, including Lotrimin\u00ae Ultra, or any other Bayer products.<\/p>\n\n\n\n
The recalled products are all packaged in aerosol spray cans. The products were distributed in the U.S., Puerto Rico, Canada and Mexico through a variety of retail channels.<\/p>\n\n\n\n
Bayer is also notifying its distributors and retailers by letter and is arranging for returns of all voluntarily recalled products. Consumers may request a refund by visiting www.lotrimin.com<\/a>External Link Disclaimer<\/a>or www.tinactin.com,<\/a>External Link Disclaimer<\/a>and may contact Bayer with questions by calling 1-866-360-3266, Monday-Friday between the hours of 8 a.m. and 8 p.m. Eastern Time. A photo of the product will be required to receive a refund. After taking your photo and completing the refund process, please discard the product appropriately. Consumers who have the products that are being recalled should stop using. Consumers should contact their physician or healthcare provider if they have any questions, concerns or have experienced any problems related to using these aerosol antifungal products.<\/p>\n\n\n\n
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail or by fax.<\/p>\n\n\n\n
- Complete and submit the report Online<\/a><\/li>
- Regular Mail or Fax: Download form<\/a> or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178<\/li><\/ul>\n\n\n\n
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.<\/p>\n","protected":false},"excerpt":{"rendered":"
Summary Company Announcement Date: October 01, 2021FDA Publish Date: October 01, 2021Product Type: DrugsReason for Announcement: Presence of benzeneCompany Name: Bayer U.S. LLCBrand Name: Lotrimin\u00ae AF and Tinactin\u00aeProduct Description: Over… <\/p>\n","protected":false},"author":8,"featured_media":50788,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[32],"tags":[751],"_links":{"self":[{"href":"https:\/\/thelehighacresgazette.com\/news\/wp-json\/wp\/v2\/posts\/50787"}],"collection":[{"href":"https:\/\/thelehighacresgazette.com\/news\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/thelehighacresgazette.com\/news\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/thelehighacresgazette.com\/news\/wp-json\/wp\/v2\/users\/8"}],"replies":[{"embeddable":true,"href":"https:\/\/thelehighacresgazette.com\/news\/wp-json\/wp\/v2\/comments?post=50787"}],"version-history":[{"count":1,"href":"https:\/\/thelehighacresgazette.com\/news\/wp-json\/wp\/v2\/posts\/50787\/revisions"}],"predecessor-version":[{"id":50790,"href":"https:\/\/thelehighacresgazette.com\/news\/wp-json\/wp\/v2\/posts\/50787\/revisions\/50790"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/thelehighacresgazette.com\/news\/wp-json\/wp\/v2\/media\/50788"}],"wp:attachment":[{"href":"https:\/\/thelehighacresgazette.com\/news\/wp-json\/wp\/v2\/media?parent=50787"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/thelehighacresgazette.com\/news\/wp-json\/wp\/v2\/categories?post=50787"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/thelehighacresgazette.com\/news\/wp-json\/wp\/v2\/tags?post=50787"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
- Regular Mail or Fax: Download form<\/a> or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178<\/li><\/ul>\n\n\n\n
- Complete and submit the report Online<\/a><\/li>