HIGH

A New Life Herbs Recalls Baby Soothe Herbal Supplement Over Misbranding

A New Life Herbs recalled 49 bottles of Baby Soothe Herbal Supplement on November 20, 2025. The product misbrands due to unapproved drug claims and lack of a Supplement Facts label. Consumers should stop using the product immediately and seek a refund.

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
INFANTS

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 recall involves Baby Soothe Herbal Supplement, packaged in a 2 oz. glass dropper bottle. It contains catnip, chamomile, vegetable glycerin, and water. The product was distributed in Alabama, Arizona, California, Georgia, Illinois, Indiana, Minnesota, Missouri, Mississippi, North Carolina, New York, and Tennessee.

The Hazard

The product features unapproved drug claims on its labeling. It also fails to provide a Supplement Facts label, which is required for dietary supplements.

Reported Incidents

There are no reported injuries or incidents associated with this recall. The misbranding and labeling issues pose a potential risk to consumers.

What to Do

Consumers should not consume the product. Contact A New Life Herbs, LLC for refund or replacement information via email.

Contact Information

For more details, consumers can visit the recall webpage at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=H-0342-2026.

Key Facts

  • 49 bottles recalled
  • Misbranding due to unapproved claims
  • No reported incidents or injuries
  • Available in multiple states
  • Contact for refunds

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Safety Assessment

Risk LevelHIGH
Severity Score
7/ 10
Affected Groups
INFANTS
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
E164BS EXP 1/27 E128BS EXP 7/26
Affected States
Nationwide
Report Date
December 31, 2025
Source Agency
FDA - Food Safety
Recall Status
ACTIVE

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