A New Life Herbs recalls Baby Soothe herbal supplement due to unapproved drug claims and missing Supplement Facts label. This affects products sold with specific expiration dates.
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
A New Life Herbs is recalling Baby Soothe herbal supplements because their labels make unapproved drug claims and lack a required Supplement Facts label. This could mislead parents about the product's safety and effectiveness.
The product has unapproved drug claims on its label, meaning it makes health claims not approved by the FDA. It also lacks a Supplement Facts label, which is required by law for dietary supplements. This could lead to incorrect use or misunderstandings about the product's safety.
Parents using Baby Soothe herbal supplements for infants may be affected. Infants with colic, upset stomach, or teething discomfort are most at risk due to potential mislabeling.
Check for the product name 'Baby Soothe Herbal Supplement' in a 2 oz. glass dropper bottle. Look for expiration dates E164BS (1/27) or E128BS (7/26) on the label.
Look for the expiration date codes E164BS (1/27) or E128BS (7/26) on the bottle.
The product has unapproved drug claims on its label and lacks a required Supplement Facts label.
Check the product label for expiration dates E164BS (1/27) or E128BS (7/26). If you have the product, you may want to contact the manufacturer for more information.
The recall is for unapproved drug claims and missing labeling, not a physical hazard. There is no risk of serious injury.
We’ve drafted a message you can send A New Life Herbs to request your refund or repair — edit it as you like.
Subject: Recall H-0342-2026 — A New Life Herbs A New Life Herbs Hello, I own a A New Life Herbs that is covered by recall H-0342-2026 from A New Life Herbs. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
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