FDA recall record
Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties, Wood Betony & White Willow in vegetable glycerin, packaged in a 4.5 oz. glass bottle or 9 oz. glass 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
Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties, Wood Betony & White Willow in vegetable glycerin, packaged in a 4.5 oz. glass bottle or 9 oz. glass bottle, UPC 231946534537
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.
Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties, Wood Betony & White Willow in vegetable glycerin, packaged in a 4.5 oz. glass bottle or 9 oz. glass bottle, UPC 231946534537
Code information listed by FDA
E170PA EXP 7/28 E174PA EXP 9/28 E161PA EXP 12/27 E146PA EXP 12/26 E123PA EXP 7/26 E110PA EXP 10/25 E93PA EXP 2/25
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: 275 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.