Boswellia Herbal Supplement, 1:5 Alcohol Double Extract

A New Life Herbs, LLC has recalled Boswellia Herbal Supplement, 1:5 Alcohol Double Extract, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on December 31, 2025 and was initiated on November 20, 2025. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Boswellia Herbal Supplement, 1:5 Alcohol Double Extract, with approximately 278 bottles affected. The company behind the recall is A New Life Herbs, LLC, based in Somerville, TN. The FDA describes the product as: “Boswellia Herbal Supplement, 1:5 Alcohol Double Extract, Extracted from Frankincense with powerful anti-inflammatory properties, useful for pain & inflammation; packaged in a 2 oz. glass dropper bottle, UPC 284260392420”

Why was Boswellia Herbal Supplement, 1:5 Alcohol Double Extract recalled?

According to the FDA, the stated reason for the recall is: “Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label.” In plain terms, this recall relates to an unapproved substance or additive.

This type of recall involves an ingredient or additive — such as a color, preservative, or other substance — that is not approved for use in the food as sold under U.S. rules. It does not automatically mean the product is harmful, but it does mean it does not meet current food regulations.

What should you do?

If you think you may have bought Boswellia Herbal Supplement, 1:5 Alcohol Double Extract, compare it against the product description and identifying codes (T848B EXP 11/30 T836B EXP 10/30 T808B EXP 9/30 T771B EXP 7/30 T723B EXP 3/30 T696B EXP 1/29 T655B EXP 10/29 T594B EXP 4/29 T536B EXP 10/28) before using it. This recall is currently listed as ongoing.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact A New Life Herbs, LLC or your local health authority.

About this recall

This recall was distributed in TN. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.