FDA recall record
Ear Drops Herbal Supplement, Mullein flower alcohol tincture 1:5, Pain relieving and antibiotic properties, packaged in a 0.5 oz. plastic dropper bottle
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of August 28, 2026. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Ear Drops Herbal Supplement, Mullein flower alcohol tincture 1:5, Pain relieving and antibiotic properties, packaged in a 0.5 oz. plastic dropper bottle
Reason
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Ear Drops Herbal Supplement, Mullein flower alcohol tincture 1:5, Pain relieving and antibiotic properties, packaged in a 0.5 oz. plastic dropper bottle
Code information listed by FDA
T553MF EXP 12/28
Distribution and firm information
Recalling firm listed by FDA: A New Life Herbs, LLC
Firm location listed by FDA: Somerville, TN, United States
Distribution reported by FDA: AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
Product quantity listed by FDA: 22 bottles
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.