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A New Life Herbs Recalls Sinus Cap Herbal Supplement Over Misbranding

A New Life Herbs recalled Sinus Cap Herbal Supplement on November 20, 2025, due to unapproved drug claims. The product lacks a Supplement Facts label, which misbrands it. Consumers should not consume the product and seek refunds or replacements.

Official notice
A New Life HerbsFood & BeveragesC136SC EXP 10/27 C128SC EXP 5/27 C110SC EXP 9/26 C109SC EXP 4/26 C102SC EXP 10/25

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA FOOD
Recall date
November 20, 2025
Status
ACTIVE
Severity
7/10

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

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Food Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
A New Life Herbs
Product type
Herbal Supplement
Model numbers
C136SC EXP 10/27 C128SC EXP 5/27 C110SC EXP 9/26 C109SC EXP 4/26 C102SC EXP 10/25
Sold at
Multiple Retailers
Where affected
Nationwide

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    November 20, 2025

  2. Reported by FDA FOOD

    December 31, 2025

  3. RecallRadar source check

    January 7, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

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

About This Product

The Sinus Cap Herbal Supplement is designed to provide relief for sinus issues using natural ingredients. Consumers often purchase herbal supplements for their perceived health benefits and alternative remedies.

Why This Is Dangerous

The product's misbranding stems from unapproved drug claims and the absence of a Supplement Facts label, which can mislead users about its effects and safety.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers face potential health risks if they consume this product, which lacks proper labeling and claims. This recall also necessitates consumers to seek refunds, causing inconvenience.

Practical Guidance

How to identify if yours is affected

  1. Check the product packaging for model numbers.
  2. Look for the absence of a Supplement Facts label.
  3. Verify the distribution states to see if your product is affected.

Where to find product info

Model numbers and expiration dates can typically be found on the packaging or label of the product.

What timeline to expect

Expect refund processing to take approximately 4-6 weeks after submission of your request.

If the manufacturer is unresponsive

  • Contact the company again via email.
  • File a complaint with the FDA or CPSC if necessary.

How to prevent similar issues

  • Always look for a Supplement Facts label when purchasing supplements.
  • Research products and their claims before buying.
  • Check for recalls on FDA website regularly.

Documentation advice

Keep a copy of your purchase receipt and any correspondence with the company for your records.

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Product Details

The Sinus Cap Herbal Supplement contains Fenugreek, Thyme, Oregon Grape Root, and Bentonite Clay. Each capsule weighs 510 mg, and the product is packaged in a plastic bag. The recall affects 38 bags distributed across Alabama, Arizona, California, Georgia, Illinois, Indiana, Minnesota, Missouri, Mississippi, North Carolina, New York, and Tennessee.

Key Facts

  • Recall date: November 20, 2025
  • Distributed in 12 states
  • No reported injuries
  • Unapproved drug claims on labeling

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
7/ 10
Affected Groups
GENERAL
Injury Types
POISONING

Product Classification

Product Details

Model Numbers
C136SC EXP 10/27 C128SC EXP 5/27 C110SC EXP 9/26 C109SC EXP 4/26 C102SC EXP 10/25
Affected States
Nationwide
Report Date
December 31, 2025
Source Agency
FDA - Food Safety
Recall Status
ACTIVE

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