UNITED STATES
Let's review your label
for the US market.
Review your US food label, Nutrition Facts, allergens and claims using FDA or USDA FSIS sources appropriate to your product category.
OUR SERVICE SCOPE
What is the next step for your product?
FDA food label review
Review existing food packaging intended for the USA for product identity, mandatory information and presentation.
Explore this serviceNutrition Facts panel review
Technical review of product data, serving-size approach, units and consistency of presentation in a US nutrition panel.
Explore this serviceUS allergen declaration review
Compare ingredient and allergen information for the US market with FDA sources.
Explore this serviceUS nutrition and product claims review
Assess the supporting evidence and scope of statements used on US packaging and in product promotion.
Explore this serviceThe right US starting point: product and jurisdiction
A US review starts with the product category, intended use and sales format. FDA sources and labelling procedures for products under USDA FSIS jurisdiction are considered separately. Importer details and the existing product dossier are included in the scope; official procedural requirements cannot be determined conclusively from a packaging image alone.
Review against current nutrition and allergen sources
The FDA notes that the nutrition and allergen chapters in its older Food Labeling Guide do not reflect all current requirements. We therefore use current Nutrition Facts resources and relevant newer allergen guidance. The source versions consulted form part of the review report.
YOUR QUESTIONS
Before we begin.
Where should I start for the USA, Gulf or another country?+
Choose your target market in the world country directory. Share your product category, current label version and importer details so we can identify the sources, documents and local verification needed for your review.
What does a label review deliver?+
You receive review notes on the existing packaging, a list of findings and recommended corrections. Design implementation, translation, laboratory analysis and official applications require a separate scope; the technical review report does not replace them.
At what stage should I seek advice?+
You can start during recipe development, with your first label draft, before printing or when entering a new market. Early assessment makes it easier to plan design and document revisions.
Which documents are needed for a label review?+
We usually start with the current label draft, recipe, ingredient specifications, available analytical reports and target-market details. The final document list depends on your product and service scope.
Can I use the same label in Türkiye and the European Union?+
This needs to be assessed for the specific product and destination country. Language, responsible operator details, product-specific provisions and national requirements may differ.
Which deliverables will I receive?+
Depending on the scope, we prepare an annotated label draft, findings and recommendations, regulatory references or a product-specific action plan. Deliverables are agreed before work begins.
Does consulting mean official product approval?+
The consulting deliverable is a technical assessment. It does not replace permission, registration or inspection by the competent authority. Relevant official procedures are identified separately for your product.
Let's talk about your product.
Tell us your target market and what you need.
Let's define the right scope of work together.