Many label problems are design problems: the right words in the wrong place, at the wrong size, on a background nobody can read. This checklist walks your designer through every panel, type size, code and proof step before the files go to the printer.
Short answer
A supplement label design puts the identity statement and net quantity on the front panel, and the Supplement Facts panel, ingredient list and business name on the front or the panel to its right. Required text needs letters at least 1/16 inch tall, most panel text 8 point, strong contrast, a bold disclaimer tied to every claim, a GS1 barcode, and a readable lot code and date.
1/16 in
minimum letter height for required information on the front and information panels
21 CFR 101.2(c)
8 pt
minimum type for most Supplement Facts text, with 6 pt for column headings and footnotes
21 CFR 101.36(e)(4)
+90 days
shelf life an FBA product needs beyond the time it takes to use it in full
Amazon, Expiration dates on FBA products
$30
one GS1 US barcode number (GTIN), with no annual renewal fee
GS1 US, How to get a UPC barcode
This is the design companion to our supplement label requirements guide, which explains what each statement must say. Here we cover where each one goes, how big it must be, and what to check on a proof. For the numbers themselves, see the Supplement Facts panel guide.
FDA's Dietary Supplement Labeling Guide, Chapter I lists five required statements: identity, net quantity, the Supplement Facts panel, the ingredient list, and the name and place of business of the manufacturer, packer or distributor. A design brief that does not place all five is not ready for a designer.
Two panels matter. The principal display panel (PDP) is the part of the package most likely to be seen at purchase, usually the front. The information panel is the panel immediately to its right. Under 21 CFR 101.2, required information goes on one of those two panels unless a rule says otherwise.
One placement rule catches many first designs. Section 101.2(e) says everything on the information panel must appear in one place without intervening material, and FDA's guide names a UPC bar code as an example. Keep the facts panel, ingredient list and business name together as one block, with the barcode, logos and marketing copy outside it. Section 101.2(d) adds that artwork and optional content do not count when judging whether a panel is too small for the required text.
Federal rules set minimums in two units: fractions of an inch for front and information panel text, and points inside the Supplement Facts panel. A label can pass one and fail the other.
The net quantity rule in 21 CFR 101.7(h) also requires bold type that contrasts with everything else on the package, measured on the lowercase o. To size it, measure the front panel: FDA's guide uses 40 percent of the circumference times the height for a round bottle. A bottle with a 7 inch circumference and a 3 inch label height has 8.4 square inches, so its net quantity needs letters at least 1/8 inch tall.
Inside the facts panel, 21 CFR 101.36(e) asks for a hairline box, a bold full-width title, one easy-to-read type style, all black or one color on a white or neutral contrasting background whenever practical, upper and lowercase letters, at least one point of leading, and letters that do not touch.
Under 21 CFR 101.15(a)(6), a required statement can lack the prominence the law requires because of small or stylized type, insufficient background contrast, obscuring designs or vignettes, or crowding. FDA's guide says the lettering does not need to be black on white, but it must contrast enough to be easy to read.
A photo, gradient or pattern behind the facts panel, ingredient list or net quantity is the obscuring vignette 101.15 warns about. Give required text a plain field.
Section 101.15(c) requires required information in English. If the label uses another language anywhere, all required information must also appear in that language.
Any statement about what an ingredient does in the body is a structure/function claim. It needs proof before you print, the FDA disclaimer, and a notice to FDA within 30 days of first marketing. Our structure/function claims guide covers the wording. Here is what each claim changes on the artwork.
Under 21 CFR 101.93(d), the disclaimer sits right next to the claim with nothing between them, or the claim ends in a symbol such as an asterisk that points to the same symbol next to the disclaimer. When the disclaimer is not adjacent, it must be set off in a box.
For one claim: This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease. For two or more claims, the plural version starts with These statements. Set it in bold, at least 1/16 inch tall (101.93(c) and (e)).
The rule says the disclaimer appears on each panel with a claim. In December 2025, FDA said it will use enforcement discretion on that each-panel part while it considers a change, but will still enforce the disclaimer on the label and its link to each claim. As of October 2026 the rule text has not changed, so the low-risk design repeats a boxed disclaimer on every panel with a claim.
FDA's disease-claim criteria include pictures and symbols. A heart with an EKG line or a glowing red joint can imply a disease claim with no words. Brief your designer before the first concepts.
Tablets and capsules with iron as an iron source need FDA's overdose warning, word for word, in a hairline box on the information panel, and on the carton too if there is one (21 CFR 101.17(e)).
Scanners, warehouses and Amazon reviewers read the barcode, lot code and date more closely than any shopper does. Get these three right before anything else on the back panel.
Amazon's valid UPCs page says Amazon checks product UPCs against the GS1 database, that UPCs not matching GS1 information are invalid, and that you should get UPCs directly from GS1 rather than resellers. It warns that invalid UPC listings will be removed. A UPC is the barcode number shoppers know; GS1 calls the number a GTIN (Global Trade Item Number).
GS1 US sells a single GTIN for $30 with no annual renewal fee, or a company prefix for larger lines, priced by item count, such as $250 to start and $50 a year to renew for 10 items. Each product variation needs its own barcode, so a 60-count and a 120-count bottle are two numbers.
FDA names the barcode as intervening material. Put it on another face, outside the facts, ingredient and business name block.
Barcodes only earn their space if they scan. In our experience the safe habits are simple: keep the barcode in proportion if it is resized, do not cut its height to save room, leave plain space on both sides of the bars, and print dark bars on a light background. Ask your printer to confirm the smallest size that scans reliably on your press and label stock.
Lot number. FDA's manufacturing rule, 21 CFR 111.415(f), requires a batch, lot or control number on each lot of packaged and labeled supplement, and Amazon's dietary supplements policy asks for label images that show identifying codes such as lot numbers. Leave a clear, uncoated window for the manufacturer's coder and agree on its location before artwork is final.
Expiration date. FDA's labeling guide says an expiration date is not required on supplements, but a date you print must be backed by valid data. Amazon is stricter for FBA. Its expiration dates on FBA products page says every ingestible product must be clearly labeled with an expiration or manufacturing date, and that lot numbers alone are not enough. At check-in, a product must have enough shelf life to be used in full plus 90 more days. Amazon's own example: a 240-serving bottle needs 330 days left. The page's guideline table lists 730 days for herbal or mineral supplements, so check which number applies to your product before you set the date format.
Amazon's accepted formats are DD-MM-YYYY (its preferred numeric format), DD-MMM-YYYY with a short month name, or MM-YYYY, which it reads as the first day of that month. Case packs and multipacks must show the date on the outer packaging and on each item inside.
On Amazon, your label is also a document. The dietary supplements policy, read in Seller Central on October 27, 2026, requires listing images that show the full English label on the product: the supplement's name, total quantity, the Supplement Facts panel and any continued panels, the ingredient list, certification logos, the identity statement, directions and any warnings. The images must also show identifying codes and the name and address of the brand owner, manufacturer, packer or distributor, and they must not include the FDA logo.
For review submissions, documents and images must be authentic, unmodified and not computer or AI generated, show all sides of the package, and show that the product is the same one tested and listed. A 3D render will not pass. Plan real photos of every side of the printed, filled bottle.
NutraIngredients reported that Amazon's updated U.S. policy rolled out March 31, 2026, with listings expected to match the Supplement Facts panel exactly. The label is now the source document for the whole listing. See Amazon supplement listing optimization for writing the listing from the panel, and the Amazon dietary supplement policy guide for the rest of the policy.
A label that wraps past the back seam may need two or three photos to show every panel. Keep the facts panel on one readable face so a single sharp photo captures it.
Amazon lists certification logos among the label elements reviewers look for. Print only seals you currently hold for this product, and keep the certificate on file.
A lot code stamped on a shiny curve can be unreadable in photos. Test the print location before the full run.
Get the final formula, serving size and directions in writing. Every label number depends on them.
Ask the printer for the exact die line (cut shape and size) for your container, and measure the front panel area from it.
Place identity and net quantity on the front, then the facts panel, ingredient list and business name together. Mark the barcode zone and lot and date window outside that block.
Check net quantity height against the 101.7(i) table, required text at 1/16 inch, facts text at 8 point or the small-package minimum, and the bold disclaimer at 1/16 inch.
Tie each structure/function claim to a boxed disclaimer, remove disease words and images, and confirm your evidence and the 30-day FDA notice plan.
Compare every amount, unit and %DV against the formula sheet, then against your Amazon draft listing. Have a second person do it separately.
Apply it to a filled bottle. Check contrast in normal light, scan the barcode, test the lot window with your manufacturer's coder, and read it around the curve.
Get the manufacturer's written approval, keep the signed proof, and after the first run photograph every side of the finished package for Amazon.
Do it yourself if your formula is simple, your manufacturer gives you a draft Supplement Facts panel, and your designer will follow this checklist and print a real proof.
Talk to a regulatory attorney if the product uses a possible new dietary ingredient, sits near drug territory such as sleep, weight, blood sugar or hormones, targets children or pregnant women, or will sell outside the U.S.
Get design help if the label is accurate but crowded or hard to read, or your Amazon listing and label do not match. That is where Evolve fits. We design supplement labels and packaging, quoted per project or done inside brand management hours. Main images, infographics and Premium A+ run $295, $495 or $595 through graphic design, and a listing rewrite built from your panel is $495 through listing optimization.
Monthly plans run Brand Support at 5 hours for $750, Brand Manager at 10 hours for $1,250, Brand Manager Plus at 20 hours for $2,000, and Full Brand Management at 40 hours for $3,600, paid upfront and month to month. See brand management for supplement brands. To have us check a proof, request a free listing audit, email Ian at [email protected], or call or text 719-257-3557. If the label is fine, we will say so.
FDA: Dietary Supplement Labeling Guide, Chapter I, General Dietary Supplement Labeling
fda.gov · Open source →
eCFR: 21 CFR 101.2, Information panel of package form food
ecfr.gov · Open source →
eCFR: 21 CFR 101.7, Declaration of net quantity of contents
ecfr.gov · Open source →
eCFR: 21 CFR 101.15, Prominence of required statements
ecfr.gov · Open source →
eCFR: 21 CFR 101.36, Nutrition labeling of dietary supplements
ecfr.gov · Open source →
eCFR: 21 CFR 101.93, Certain types of statements for dietary supplements
ecfr.gov · Open source →
Amazon Seller Central: Dietary supplements policy
sellercentral.amazon.com · Open source →
Amazon Seller Central: Valid UPCs
sellercentral.amazon.com · Open source →
Amazon Seller Central: Expiration dates on FBA products
sellercentral.amazon.com · Open source →
GS1 US: How to get a UPC barcode
gs1us.org · Open source →


Founder, Evolve Media Agency
Ian has run Evolve Media Agency since 2017 and has sold on Amazon since 2015. He and Megan run brand management, launches, PPC and in-house photo and video for Amazon, Shopify and TikTok Shop brands, including supplement brands, from Colorado. Questions about this page go straight to him at [email protected].
Guide
What each required statement must say, with the regulation behind it.
Guide
How to write a claims-safe title, bullets and backend keywords from your label.
Service
One team keeping label, listing, images and launch in line with each other.
Free · 30 minutes · No pitch deck
Book a free 30-minute call and bring your label proof and ASIN. We will check placement, sizes, claims and the Amazon match, and tell you what to fix before you print.
Rather email? Write Ian at [email protected]. Call or text 719-257-3557. Watch our YouTube channel, grab the free Ecom Profit Box guides, or join the newsletter.
Tell us what you sell and where you are stuck. Ian replies within one business day, and you get an email right away with a link to book a free 30-minute call.
Rather talk now? Call or text 719-257-3557 or pick a time on Calendly.