Moderate riskFDA FoodClass II

A New Life Herbs Pain Away recalled for unapproved drug claims

A New Life Herbs' Pain Away herbal supplement contains labeling that makes drug claims (like "analgesic" and "anti-inflammatory") without FDA approval. The product also lacks a required Supplement Facts label, making it misbranded. About 275 bottles were distributed across 13 states.

From the FDA notice · Read the official notice ↗

What to do

  1. Stop using Pain Away if you have a bottle with UPC 231946534537 or batch codes E170PA through E93PA
  2. Do not take this product
  3. Contact A New Life Herbs, LLC or your retailer for a refund or disposal instructions

Is yours affected?

Compare your label or packaging with the recalled product.

Product
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
UPC code
  • 231946534537
Sold in
AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
Made for
Adults

This recall covers 9 products — see all of them.

Details

Units affected
275 bottles
Illnesses reported
None reported
Manufactured in
17745 Us Highway 64, N/A, Somerville, TN, United States
Classification
Class II
Recall number
H-0347-2026

In the FDA's words

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 Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label 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: AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN Affected quantity: 275 bottles
Hazard
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label

9 products in this recall

A New Life Herbs supplements recalled for unapproved drug claims

A New Life Herbs is recalling nine herbal supplement products sold as alcohol tincture, capsule, and dropper-bottle products, including products for immune, pain, sinus, and baby-care use. The FDA says the labels make unapproved drug claims and the products lack a Supplement Facts label. The products were distributed in AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, and TN, and no injuries have been reported.

The agency lists each product separately. Check every one you might have.

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