FDABridge
← Balik sa blog
Pangunahing Pangunahing Pangunahing Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Panguna

FDA 이야기 #020 — 아르헨티나 와이너리가 미국이 완전히 다른 형식을 요구한다는 것을 알기 전에 라벨에 $11,000를 썼다

와인 라벨이 인쇄되었습니다. 30,000병. 그런데 수입업자가 말했습니다: 미국 와인 라벨링은 FDA가 아닌 TTB가 규제합니다 — 라벨이 둘 다 준수하지 않았습니다.

Koponan ng FDABridgeEne 1, 20263 min na mabasa

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.

문제

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.

비용

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.

FDABridge가 도와드립니다

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.

Kailangan mo ng tulong sa susunod?

Kailangan ng tulong sa pagpili ng serbisyo?

Ihambing ang mga serbisyo at piliin ang tamang filing path para sa iyong produkto.

Mas marami pang mabasa

Mga kaugnay na artikulo

Pangunahing Pangunahing Pangunahing Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Panguna

의료기기 라벨링 기호: 미국 시장 진입을 위해 해외 제조업체가 알아야 할 사항

Abr 28, 2026

미국의 의료기기 라벨링에는 적절한 통신을 위해 특정 기호가 필요합니다. 해외 제조업체는 미국 시장에 기기를 수출하기 전에 FDA가 수용하는 기호 기준을 이해해야 합니다.

Magbasa pa →
Pangunahing Pangunahing Pangunahing Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Panguna

해외 제조업체를 위한 의료기기 등록: 미국 규제 시스템 가이드

Mar 26, 2026

해외 의료기기 제조업체는 사업소를 등록하고, 기기를 목록에 등록하며 — 기기 등급에 따라 — 미국에서 유통하기 전에 FDA 허가 또는 승인을 받아야 합니다.

Magbasa pa →
Pangunahing Pangunahing Pangunahing Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Pangunahang Panguna

FDA 상담자 를 고용 하기 전 에 질문 할 수 있는 10 가지 질문

May 24, 2026

FDA의 준수 서비스 제공자를 선택하는 것은 중요한 결정입니다. 이 10가지 질문은 외국 제조업체가 능력 있는 컨설턴트를 해결할 수 없는 문제들을 만들어내는 사람들로부터 분리시키는 데 도움이 됩니다.

Magbasa pa →