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FDA Warning Letter · #700358

Www24Hreupbiz: FDA Warning Letter (April 23, 2025)

Www24Hreupbiz received this warning letter on April 23, 2025, from FDA’s Center for Drug Evaluation and Research (CDER). What it cites, and FDA’s own words where we matched them against the letter, are summarized below.

Issued April 23, 2025Status: activeCenter for Drug Evaluation and Research (CDER)On this register since August 16, 2026
By Ruth Calder · Enforcement Editor
Editorially reviewed. Not medical advice · How we verify contentLast reviewed

Primary Source

View the original FDA letter on fda.gov →

https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/warning-letters/www24hreupbiz-700358-04232025

Summary

Company
Www24Hreupbiz
Letter number
#700358
Issue date
April 23, 2025
Subject
Not listed by FDA for this letter

What FDA cited

FDA's letter of April 23, 2025 cites Www24Hreupbiz for selling products FDA calls unapproved new drugs. The GLP-1 drugs it names: semaglutide.

In FDA’s words:
As discussed below, FDA has observed that www.24hreup.biz introduces into interstate commerce unapproved and misbranded semaglutide drug products. … FDA has observed that www.24hreup.biz offers “Ozempic 0.5mg,” “Ozempic 1mg,” and “Rybelsus Semaglutide 14mg” for sale without a prescription.

How this letter sits against the other 159

Our reading, from the 160 letters on this register — not part of the FDA’s document.

No other letter on this register carries the date April 23, 2025. The agency acted against this company on its own that day, which is uncommon here — most of the letters we hold arrived in sweeps.

A warning letter is the agency putting a company on notice, not a court finding and not a ban. What it is worth to you is in what it alleges, so read the original on fda.gov rather than the fact that one exists.

For checking a pharmacy website before you order: How to verify an online GLP-1 pharmacy: six public checks.

FDA’s letter of May 5, 2025 to Wwwpeacefulmedscom also cites its recipient for selling products FDA calls unapproved new drugs.

What FDA warning letters mean

It is the agency writing to a company to say it believes something that company is doing breaks the Federal Food, Drug, and Cosmetic Act — usually a claim on a website, a labeling choice, or how a drug is being made. The company has about fifteen working days to write back.

Read carefully what it is not. It is not a recall, not a criminal charge, and not a court deciding anyone broke the law. It is the regulator opening a file. Companies frequently answer a letter, fix what was cited, and carry on trading, and when FDA accepts that it can issue a close-out letter. We do not track close-outs, so the presence of a letter on this page tells you what FDA said on one date — not where the matter stands today. Ask the company; they will usually tell you, and how they answer is informative in itself.

Across this market the same three citations recur: claiming a compounded product is equivalent to an approved one, labeling that misleads, and compounding from bulk substances FDA has not cleared under sections 503A and 503B. If you are reading a letter here, it is probably one of those.

Where to get GLP-1 online, safely: sellers our editors have checked

These are telehealth sellers our editors have checked. For each one we hold a price, the form the drug comes in, and the states it reaches.

No insurance needed · vetted by our editors

Some of the links on this page earn us money. If you sign up with a provider after following one, that provider may pay GLP Watchdog a commission. Learn more

8.2

bmiMD

Starting below a standard dose, with microdose tiers

9.1

Collective

Flat any-dose pricing, if you can absorb a $199 annual membership on top

From $59/mo + membership

Get started →
Read full review →
9.3

Embody

A flat compounded tirzepatide or semaglutide price at every dose, from a seller that names its pharmacies

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Editorial Disclaimer

This is a public communication from a regulator, and by itself it settles nothing about whether the company broke any law. Corrective action is a common response, and a fair number of letters end in a close-out. Read the whole thing on fda.gov through the link above rather than taking our excerpt as the full picture.

Glossary

The words sellers use, defined. Tap any term.