Class IITerminated in FDA datasetRecall initiated Nov 20, 2025

Pain Away Herbal Supplement, Analgesic & anti-inflammatory properties, Wood Betony & White…

Recalling firm: A New Life Herbs, LLC

Why it was recalled

Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Aug 28, 2026.

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ProductPain 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
Package size4.5 oz
UPC231946534537

FDA code information

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

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Full FDA record and distribution details

Original product description

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

Extracted codes and context

TypeCode / valueContext
UPC231946534537getable glycerin, packaged in a 4.5 oz. glass bottle or 9 oz. glass bottle, UPC 231946534537

Original FDA recall reason

Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label

Recall details

Recall number
H-0347-2026
Event ID
98037
FDA status
Terminated
Initiated
Nov 20, 2025
Reported
Dec 31, 2025
Classified
Dec 23, 2025
Terminated
Aug 28, 2026
Quantity
275 bottles
Location
Somerville, TN, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN

FDA source record · H-0347-2026

Data updated September 16, 2026. View official FDA data ↗

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