For Supplement startups

FDA Supplement Facts Label Generator for Supplement Startups

Prepare your first Supplement Facts draft with a clear distinction between supplier data, example data and your final reviewed product.

Source → review → panel draft
Supplement Facts
Serving Size 2 Gummies
Servings Per Container 30
Amount Per Serving
%DV
Vitamin A (as Beta-Carotene)
900 mcg RAE
100%
Vitamin C (as Ascorbic Acid)
60 mg
65%
Vitamin D3 (as Cholecalciferol)
20 mcg
100%
Vitamin E (as d-Alpha Tocopherol)
15 mg
100%
Vitamin B6 (Pyridoxine HCl)
2 mg
118%
Folate (as Methylfolate)
400 mcg DFE
100%
Vitamin B12 (Methylcobalamin)
6 mcg
250%
Iodine (Potassium Iodide)
150 mcg
100%
Zinc (as Zinc Citrate)
11 mg
100%
Selenium (Selenomethionine)
55 mcg
100%
Choline (Choline Bitartrate)
25 mg
5%
* Percent Daily Values are based on a 2,000 calorie diet.
Other Ingredients: Glucose syrup, sugar, pectin, citric acid, coconut oil.
Contains: Tree Nuts (coconut).
Illustrative sample · Replace example values with your own confirmed data
A practical workflow

From a first specification to a designer brief

A founder has a capsule specification but no finished facts-panel artwork.

  1. Confirm whether quantities describe one capsule or the complete serving.
  2. Inspect source forms, dietary ingredient rows and Other Ingredients together.
  3. Review the label draft, confirm a version, and share the output with the packaging designer.

A reviewed panel and its source specification make a concrete design brief; the complete package still needs its own review.

Explore this example with its source values →

From specification to usable artwork

Extract and inspect

Upload a supported document or enter confirmed values. Compare the extracted fields with the original before accepting them.

Review the panel

Check serving details, ingredient identity, units and the selected layout. Missing values stay unresolved until you supply the data.

Hand off your files

Export PDF, SVG or PNG artwork plus JSON and XML data from a confirmed, unlocked label version.

01

Choose the product type

Confirm the intended use, presentation and product category before selecting Supplement Facts. A liquid or gummy form alone does not establish classification. The food and supplement workflows use different declaration and layout rules.

02

Collect declared values

Request the actual finished-product serving size, servings per container and ingredient amounts. A raw-material COA or formula percentage may need additional information before it can become a declared amount per serving. Leave unknown values unresolved until you have supporting data.

03

Build and compare

Enter confirmed values manually or import a supported document, then compare the extracted fields with the source. Check units, population and ingredient identities. A template can show panel structure, but its amounts must not be mistaken for your product specification.

04

Launch review

Inspect the full label draft and the complete package with your reviewer before confirming. Free exploration does not require purchasing a plan. Review the current price and version rules before unlocking files; confirming and downloading a panel does not constitute FDA approval.

Files, revisions and purchase

Create and edit a draft before choosing a paid export. New-account credits can unlock watermark-free exports; see Pricing for the registration offer. Paid export formats are PDF, SVG, PNG, JSON and XML. An unlocked confirmed label can be downloaded again without another credit. Changes require a new draft version, review and confirmation; unlocking that new version uses another credit or active Pro access. Compare current plans and billing details.

Source and review checklist

Prepare the required product data, compare layout conditions, and consult ingredient references. Check the final panel against its source and review the complete package before use.

Regulatory references: 21 CFR 101.36 and ingredient labeling, 21 CFR 101.4. These references describe labeling requirements; they do not certify this example or approve a marketplace listing. Content reviewed October 20, 2026.

Explore other use cases → · How we handle review and data →