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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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.

The Hazard

The product contains unapproved drug claims on its labeling. It is misbranded due to the omission of a Supplement Facts label.

Reported Incidents

No injuries or incidents have been reported in relation to this recall. The product poses a high risk due to misleading labeling.

What to Do

Consumers should stop using the product immediately. Contact A New Life Herbs, LLC for refund or replacement information via email.

Contact Information

For refunds, contact A New Life Herbs, LLC. Email notifications will be sent to consumers who purchased the product.

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

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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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