A New Life Herbs Ginger Supplement Recall: Unapproved Drug Claims
A New Life Herbs recalls organic ginger root supplements due to unapproved drug claims and missing Supplement Facts label. Consumers should check packaging for expiration dates and contact the company for details.
Lower-risk recall
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
Contact the company
What happened, in plain English
A New Life Herbs is recalling organic ginger root supplements because their labeling makes unapproved drug claims and lacks a required Supplement Facts label. This could mislead consumers about the product's health effects. Read more at govinfonow.com/recall/6956-a-new-life-herbs-ginger-supplement-recall-unapproved-drug-claims.
Source Summary by GovInfoNow · govinfonow.com/recall/6956-a-new-life-herbs-ginger-supplement-recall-unapproved-drug-claims · Updated August 17, 2026 · Official notice: FDA #H-0346-2026
Cite this page
“A New Life Herbs Ginger Supplement Recall: Unapproved Drug Claims.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/6956-a-new-life-herbs-ginger-supplement-recall-unapproved-drug-claims. Based on FDA recall #H-0346-2026.
Why it’s dangerous
The product has unapproved drug claims on its label, meaning it suggests health benefits that aren't approved by the FDA. It also lacks a Supplement Facts label, which is required by law for dietary supplements.
Who’s affected
Anyone who purchased this supplement from a retailer. People using it for health reasons may be at risk of being misled about its effects.
How to tell if you have this one
Check the product packaging for expiration dates like C132GR EXP 7/27 or similar codes. The product is sold as a 50-capsule supplement with a plastic bag packaging.
- Brand
A New Life Herbs- Category
Food
All 9 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Terminated- Distribution
AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| H-0340-2026 | Anti-virus Herbal Supplement, 1:5 Alcohol Tincture, Helps to stop viral replication, expectorant properties, Contains: Forsethia blossoms, Sumac berries, Pine needles; packaged in a 2 oz. glass dropper bottle, UPC 283162814429; T801AV EXP 9/30 T686AV EXP 12/29 T636AV EXP 9/29 T564AV EXP 9/28 | 116 bottles |
| H-0341-2026 | Baby Allergy Herbal Supplement, Contains: Echinacea Purpurea, Oregon Grape Root, Dandelion & Burdock Root, Fenugreek, Ginger Root in vegetable glycerin; packaged in a 2 oz. glass dropper bottle, UPC 249953949282; E166SA EXP 4/28 | 23 bottles |
| H-0342-2026 | Baby Soothe Herbal Supplement, Promotes rest, helps ease colic, upset stomach, and teething discomfort, Contains: Catnip, Chamomile, Vegetable Glycerin, water; packaged in a 2 oz. glass dropper bottle; E164BS EXP 1/27 E128BS EXP 7/26 | 49 bottles |
| H-0343-2026 | 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; 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 | 278 bottles |
| H-0344-2026 | Chaga Mushroom Herbal Supplement, 1:5 Alcohol Double Extract, Supports a healthy immune system with anti-cancer properties; packaged in a 2 oz. glass dropper bottle, UPC 284588087831; T720CH EXP 3/30 T656CH EXP 10/29 T618CH EXP 7/29 T568CH EXP 1/29 T532CH EXP 10/28 | 144 bottles |
| H-0345-2026 | Ear Drops Herbal Supplement, Mullein flower alcohol tincture 1:5, Pain relieving and antibiotic properties, packaged in a 0.5 oz. plastic dropper bottle; T553MF EXP 12/28 | 22 bottles |
| H-0346-2026 | Organic Ginger Root Herbal Supplement, Natural anti-inflammatory properties, supports gut, increases circulation, 50 capsules/560 mg, packaged in a plastic bag; C132GR EXP 7/27 C131GR EXP 6/27 C121GR EXP 2/27 C115GR EXP 12/26 C108GR EXP 1/26 C93GR EXP 7/25 | 48 bags |
| H-0347-2026 | 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; 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 | 275 bottles |
| H-0348-2026 | Sinus Cap Herbal Supplement, Herbs containing antibiotic, drying, expectorant, and emollient properties, Fenugreek, Thyme, Oregon Grape Root, & Bentonite Clay, 50 capsules/510 mg; packaged in a plastic bag; C136SC EXP 10/27 C128SC EXP 5/27 C110SC EXP 9/26 C109SC EXP 4/26 C102SC EXP 10/25 | 38 bags |
What to do — step by step
Check Product Label
Look for expiration dates on the packaging, such as C132GR EXP 7/27.
Where it went and when
Where it was distributed
Distributed in 12 states.
FDA distribution: “AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Arizona, California, Georgia, Illinois, Indiana, Minnesota, Mississippi, Missouri, New York, North Carolina, Tennessee.
Recall timeline
FDA terminated this recall 9 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #H-0346-2026 (November 20, 2025)
- Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.