Bebidas prontas, mixers, energéticos, funcionais - todas as regras de bebidas cobertas
Bebidas têm sua própria escada de RACC (§ 101.12 Tabela 2) e convenções de arredondamento diferentes. A declaração de açúcar dispara advertências distintas em mercados distintos.
RACC de bebidas + convenções de porção
Água e bebidas prontas usam por padrão a porção de 240 mL / 8 fl oz. Concentrados usam 30 mL. Energy shots têm a sua própria. Escolhemos a RACC automaticamente da tabela da FDA.
Limiares FOP específicos de bebidas
O octógono de açúcar do México dispara com ≥ 5% da energia para bebidas (vs 10% para sólidos). O "ALTO EN AZÚCARES" do Chile dispara com 5 g/100 mL. Aplicamos a escada específica de bebidas para cada mercado com FOP.
Divulgações de cafeína + edulcorantes
Os retângulos da Ley 27.642 argentina para "CONTIENE CAFEÍNA" e "CONTIENE EDULCORANTES" disparam quando aplicável. Divulgações semelhantes no Equador, Peru e Uruguai.
Gestão de SKUs multissabor
10 sabores da mesma base? Salve a base, duplique + ajuste a essência do sabor e gere 10 rótulos. As listas de ingredientes se ajustam automaticamente por SKU.
If it contains juice, you owe a percentage declaration
A beverage that purports to contain juice - by name, by image, or by implication - has to declare its percentage juice content under 21 CFR § 101.30. This catches more products than people expect, because the trigger is what the package suggests rather than what the formula contains.
A sparkling water with a lime on the front and no juice in the bottle raises the question. A "berry" flavoured drink with two percent juice has to say two percent. The declaration sits near the top of the information panel, and it is a common finding in warning letters precisely because brands treat the fruit imagery as marketing rather than as a claim.
Is your energy drink a beverage or a supplement?
This is the single biggest fork in beverage labeling, and brands sometimes pick a side without realising they have.
A product marketed as a conventional beverage carries a Nutrition Facts panel under § 101.9, uses food additives that are permitted for that use, and cannot carry structure/function claims freely. A product marketed as a liquid dietary supplement carries a Supplement Facts panel under § 101.36, operates under DSHEA, and takes the structure/function disclaimer.
What decides it is not the format of the container. The FDA looks at how the product is represented - its name, its labeling, its marketing, the serving size, the packaging format, and whether it is positioned as something you drink for refreshment or take for an effect. A 16 oz can sold in the chiller next to soft drinks reads as a beverage no matter what the panel says.
Getting this wrong means the wrong panel, potentially the wrong permitted ingredients, and claims you are not entitled to make. It is worth deciding deliberately, early, and documenting the reasoning.
If there is alcohol in it, the FDA may not be your regulator
Most alcoholic beverage labeling falls to the TTB - the Alcohol and Tobacco Tax and Trade Bureau - under the Federal Alcohol Administration Act, not to the FDA. That covers distilled spirits, wine above the statutory threshold, and malt beverages made from malted barley and hops.
But the split is not clean, and the exceptions are exactly where the modern drinks market lives. Certain low-alcohol wines, ciders below the threshold, and beers brewed without malted barley or without hops can fall outside TTB's remit and back under the FDA - which means a Nutrition Facts panel and FDA ingredient labeling rather than TTB requirements.
Hard seltzers, sake-based products, and gluten-free beers made from sorghum or rice are the usual candidates for this confusion. If you are anywhere near that boundary, confirm which agency governs your product before you commission artwork, because the two regimes want genuinely different labels.