HIGH

A New Life Herbs Recalls Baby Allergy Herbal Supplement Over Label Issues

A New Life Herbs, LLC recalled 23 bottles of its Baby Allergy Herbal Supplement on November 20, 2025. The recall follows unapproved drug claims and absence of a Supplement Facts label on the product. Consumers should not consume the supplement and should seek refunds immediately.

Quick Facts at a Glance

Recall Date
November 20, 2025
Hazard Level
HIGH
Brand
A New Life Herbs
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
Nationwide (50 states)
At-Risk Groups
GENERAL

Hazard Information

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

What You Should Do

Consumers who have purchased this product should not consume it. Contact A New Life Herbs, LLC for refund or replacement information. Notification method: E-Mail

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About This Product

This Baby Allergy Herbal Supplement is marketed to alleviate allergy symptoms in infants using herbal ingredients. Consumers typically buy it for its natural approach to allergy relief.

Why This Is Dangerous

The product is dangerous due to unapproved drug claims that mislead consumers about its effectiveness. The lack of a Supplement Facts label means that consumers cannot verify the ingredients or their dosages.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

The recall may cause inconvenience for parents seeking allergy relief for their infants. Consumers need to act quickly to avoid potential health risks.

Practical Guidance

How to identify if yours is affected

  1. Check if your product matches the UPC 249953949282.
  2. Look for labels indicating Supplement Facts on the bottle.
  3. Review your purchase records to confirm if you bought the product.

Where to find product info

The UPC can usually be found on the bottom of the bottle or on the packaging.

What timeline to expect

Expect refund processing to take 4-6 weeks once your request is submitted.

If the manufacturer is unresponsive

  • Document your request with dates and details.
  • Follow up with another email or call.
  • If still unresponsive, consider reporting to the FDA.

How to prevent similar issues

  • Look for dietary supplements with clear Supplement Facts labels.
  • Check for FDA approval indications on herbal products.
  • Research brands and read reviews before purchasing.

Documentation advice

Keep a copy of your purchase receipt, any emails sent to the company, and photographs of the product.

Product Details

The recalled product is packaged in a 2 oz. glass dropper bottle. The UPC is 249953949282. It was distributed in Alabama, Arizona, California, Georgia, Illinois, Indiana, Minnesota, Missouri, Mississippi, North Carolina, New York, and Tennessee.

Key Facts

  • 23 bottles recalled
  • Unapproved drug claims on labeling
  • No Supplement Facts label present
  • Distributed in 12 states
  • Contact A New Life Herbs for refunds

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
E166SA EXP 4/28
Affected States
Nationwide
Report Date
December 31, 2025
Source Agency
FDA - Food Safety
Recall Status
ACTIVE

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