FDABridge
← Retour au blog
Général

FDA कहानियाँ #020 — अर्जेंटीना की वाइनरी ने लेबल पर $11,000 खर्च किए इससे पहले कि पता चले कि अमेरिका को पूरी तरह अलग प्रारूप चाहिए

वाइन लेबल छप गए। 30,000 बोतलें। फिर आयातक ने बताया: अमेरिकी वाइन लेबलिंग TTB द्वारा विनियमित है, FDA द्वारा नहीं — और उनके लेबल दोनों का अनुपालन नहीं करते।

Équipe FDABridge1 janv. 20263 min de lecture

A boutique winery in Mendoza, Argentina, had spent months preparing their first export to the United States. A Malbec and a Torrontés — two wines with strong US market appeal. They hired a designer in Buenos Aires, worked through multiple iterations, and printed 30,000 labels. Total printing cost: $11,000.

Then their US importer reviewed the labels.

समस्या

Wine, beer, and spirits in the United States are not primarily regulated by the FDA. They fall under the jurisdiction of the Alcohol and Tobacco Tax and Trade Bureau (TTB), a division of the US Department of the Treasury. TTB has its own labeling requirements under 27 CFR Parts 4, 5, and 7 — and those requirements are completely different from FDA food labeling rules. The Argentinian winery had designed their labels based on general FDA food labeling guidance they found online. None of it applied.

TTB requires a Certificate of Label Approval (COLA) before any wine can be sold in the United States. The COLA application requires specific label elements: brand name, class/type designation (e.g., 'Red Wine' or 'Malbec'), appellation of origin, alcohol content, net contents, name and address of the importer, country of origin, sulfite declaration, and a government health warning statement with specific prescribed language. The winery's labels were missing the health warning, had the alcohol content in the wrong format, lacked the importer's name and address, and did not include the sulfite declaration.

लागत

All 30,000 labels were unusable. They could not be modified or stickered over — the health warning and several other mandatory elements had to be integrated into the label design, not added as aftermarket patches. The winery had to redesign the labels from scratch, resubmit to the printer, and wait for a new production run. The reprint cost an additional $11,000. The launch was delayed by seven weeks.

FDABridge आपकी मदद करता है

FDABridge specializes in FDA-regulated products — food, cosmetics, drugs, and dietary supplements. Wine, beer, and spirits are primarily TTB-regulated, not FDA-regulated. When this winery contacted us, we identified the jurisdictional issue immediately and referred them to a TTB compliance specialist. We do this whenever a client's product falls outside FDA jurisdiction — we tell you honestly and connect you with the right resource.

But here is what this story teaches: before you print a single label, before you spend a dollar on design, know which US agency regulates your product. If it is food, cosmetics, drugs, or supplements — we handle it. fdabridge.com/contact. If it is alcohol or tobacco — you need a TTB specialist, and we will tell you that before you waste your money.

Besoin d'aide pour la suite ?

Need help choosing a service?

Compare the main service options and choose the filing path that fits your product category.

À lire aussi

Articles connexes

Général

Symboles de marquage des dispositifs médicaux: Ce que les fabricants étrangers doivent savoir pour entrer sur le marché américain

28 avr. 2026

L'étiquetage des dispositifs médicaux aux États-Unis nécessite des symboles spécifiques pour une bonne communication. Les fabricants étrangers doivent comprendre les normes de symboles acceptées par la FDA avant d'exporter les appareils sur le marché américain.

Lire la suite →
Général

Enregistrement des dispositifs médicaux pour les fabricants étrangers: Un guide du système de réglementation américain

26 mars 2026

Les fabricants étrangers de dispositifs médicaux doivent enregistrer leurs établissements, répertorier leurs dispositifs et, selon la classe de dispositifs, obtenir l'approbation ou l'approbation de la FDA avant de les distribuer aux États-Unis.

Lire la suite →
Général

Dix questions à se poser avant d'embaucher un consultant de la FDA

24 mai 2026

Le choix d'un fournisseur de services de conformité de la FDA est une décision conséquente. Ces dix questions aident les fabricants étrangers à séparer les consultants compétents de ceux qui vont créer des problèmes qu'ils ne peuvent pas résoudre.

Lire la suite →