A New Life Herbs recalls Pain Away herbal supplements due to unapproved drug claims and missing Supplement Facts label. Consumers should check product details and contact the company for guidance.
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
A New Life Herbs is recalling Pain Away herbal supplements because the product labels make unapproved drug claims and lack a required Supplement Facts label. This could mislead consumers about the product's health effects.
The product contains unapproved drug claims on its label, which means it may be marketed as a medicine without proper FDA approval. The missing Supplement Facts label also fails to provide necessary nutritional information, potentially leading to confusion about the product's health effects.
Anyone who purchased the Pain Away herbal supplement in glass bottles (4.5 oz or 9 oz) with the specified UPC code. People using the product for pain relief may be at risk of being misled by the labeling.
Check for glass bottles labeled 'Pain Away Herbal Supplement' with 4.5 oz or 9 oz capacity. The product has a specific UPC code (231946534537) and expiration dates listed on the label.
Look for the product's UPC code (231946534537) and expiration dates on the label to confirm if it's recalled.
The recall is due to unapproved drug claims and missing Supplement Facts label, not safety concerns. The product may still be safe but could mislead consumers about its health effects.
Check for glass bottles labeled 'Pain Away Herbal Supplement' with 4.5 oz or 9 oz capacity and the UPC code 231946534537.
The recall does not specify a remedy, so contact A New Life Herbs directly for guidance.
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-0347-2026 — A New Life Herbs A New Life Herbs Hello, I own a A New Life Herbs that is covered by recall H-0347-2026 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.
