---
title: "Boswellia Herbal Supplement, 1:5 Alcohol Double Extract, Extracted from Frank... — FDA record H-0343-2026 | Is It on Recall"
description: "Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label"
url: https://isitonrecall.com/recall/fda-food-h-0343-2026-boswellia-herbal-supplement-1-5-alcohol-double-extract-extracted-from-frankincense-with-powerful-ant/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA food enforcement

# Boswellia Herbal Supplement, 1:5 Alcohol Double Extract, Extracted from Frankincense with powerful anti-inflammatory ... — FDA record H-0343-2026

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Nov 20, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: 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
- **Reason**: Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- **Classification**: Class II
- **Recalling firm**: A New Life Herbs, LLC
- **Quantity**: 278 bottles
- **Agency-reported status**: Terminated
- **Source record identifier**: H-0343-2026

[Open the official record](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0343-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | 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 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

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

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Alabama](https://isitonrecall.com/state/alabama/)
- [Arizona](https://isitonrecall.com/state/arizona/)
- [California](https://isitonrecall.com/state/california/)
- [Georgia](https://isitonrecall.com/state/georgia/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Indiana](https://isitonrecall.com/state/indiana/)
- [Minnesota](https://isitonrecall.com/state/minnesota/)
- [Missouri](https://isitonrecall.com/state/missouri/)
- [Mississippi](https://isitonrecall.com/state/mississippi/)
- [North Carolina](https://isitonrecall.com/state/north-carolina/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Tennessee](https://isitonrecall.com/state/tennessee/)

## Dates in the source

- **Report date**: Dec 31, 2025
- **Recall initiation date**: Nov 20, 2025
- **Center classification date**: Dec 23, 2025
- **Termination date**: Aug 28, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0343-2026%22)

## Related records

[Other food records](https://isitonrecall.com/category/other-food/) [A New Life Herbs, LLC records](https://isitonrecall.com/brand/a-new-life-herbs-llc/)