Arbitr
Use cases▾
PlatformPricing
Resources▾
Explore
About▾
The company
Book a demo
Home > Regulations > MoCRA Cosmetics Labeling Rules (FD&C Act 609)

Modernization of Cosmetics Regulation Act of 2022 (FD&C Act section 609)

The US MoCRA cosmetics labeling rules

For cosmetics brands selling in the US working out what MoCRA added to labels, and what is still to come. This page covers what you need to know and ways to avoid running into issues.

What we've seen reported

MoCRA's cosmetics labeling rules, added to the FD&C Act by the Modernization of Cosmetics Regulation Act of 2022, put an adverse event contact and, for salon products, a professional-use statement on labels, with fragrance allergens to follow.1,2

Last updated October 2026 · General information only, not legal advice. Sources.

Who it covers
Responsible persons: the manufacturer, packer or distributor named on the label, according to its text1
Applies from
December 29, 20241Professional-use statement since December 29, 2023; fragrance allergens await an FDA rule2
Region
United States1

What the rules cover

What the rules ask for

These are the label items MoCRA's cosmetics labeling rules describe, according to the Act and FDA, and where each is described as applying.1,2,3

RequirementWhere it applies
Adverse event contact detailsA domestic address, phone number or electronic contact, such as a website, for adverse event reports.
Professional-use productsA clear and prominent statement that only licensed professionals administer or use the product.
Professional-use products: other label informationThe same label information the Act describes for cosmetics sold to consumers.
Who counts as a licensed professionalIndividuals licensed by a state in cosmetology, nail care, barbering or esthetics.
The responsible personThe manufacturer, packer or distributor whose name appears on the label.
Fragrance allergensTo be listed on labels once FDA sets them by regulation; no rule yet.
Existing cosmetic label rulesIngredients, net quantity and warnings under FDA rules and the FPLA continue alongside.

Where it goes wrong

Approved once. Then it drifts.

One approved set of product information ends up in many channels, markets and languages. Along the way it gets shortened, translated and reworded, and some versions end up without the warnings or details these rules require.

Approved onceIllustrative example

Heldan Pro bond treatment: US adverse event contact (phone and website) and "For use only by licensed professionals"

  • Salon bottle · USProfessional-use statement and US contact line
  • Marketplace listing · USDriftedResold to consumers; label photo croppedProfessional-use statement missing
  • Website · USContact page linked from the label
  • Imported travel size · USDriftedEU address only on the packUS adverse event contact missing
  • Distributor sell sheet · USLabel artwork with both statements
  • Website · US SpanishSolo para uso profesional; contacto en EE. UU. "Professional use only; US contact"

How Arbitr helps

So how do you keep cosmetics labels under control across every market and channel?

Read every version by hand? Or use AI to check what you publish against what you've already approved.

Check everything manually?

  • Too much to check. More versions go out every week than anyone can read in every language.
  • Drift goes unseen. No way of knowing when an approved product information has changed.
  • Changes mean starting over. No easy way to re-check what's live when your approved rules, claims or terms change.

Let Arbitr do it for you

  • Scan what's live. Go through every live version, in every language, against your approved rules, and find every label and listing missing the adverse event contact or professional-use statement.
  • See what needs attention. See each flagged version with the rule behind it, so your team decides what changes.
  • Check what comes next. Check new content against what you approved before it goes live, in every channel, market and language.

Approve once. Apply everywhere.

FAQ

Questions about the US MoCRA cosmetics labeling rules

For your teams
Where do MoCRA label details go missing?

Usually where a label is reused rather than redesigned. MoCRA's cosmetics labeling rules describe a domestic contact for adverse event reports and a professional-use statement,1 and we usually find gaps in:

  • imported and travel-size packs
  • salon products resold online
  • marketplace photos that crop the back label
  • private-label and gift-set packs
  • Spanish-language packs and pages
How do imported products pick up a US adverse event contact?

Plan it as part of the US label set, not a sticker added at the border. Global artwork often carries only a European or Asian address, so record the approved US contact line once and check every pack size against it. Our packaging and labels page shows how teams keep label sets in step.

What goes in the record for each cosmetic label?

Keep one record per product: the approved contact line, any professional-use statement, the ingredient list, who approved each, and every pack, listing and feed it appears on. When the contact details or a formula change, the record shows which versions still carry the old ones.

How it applies to a specific label is a question for your legal adviser. Where that label appears across your markets and languages is a question Arbitr answers.

Who needs to know about MoCRA cosmetics labeling?

Regulatory teams usually own it, but packaging, e-commerce, salon sales and distributors all publish labels, and resellers republish them. A short briefing for each, using your own packs, helps. Rules for other markets, such as UKCA marking for Great Britain, are on our product labeling hub.

About the rules
When did the MoCRA labeling requirements take effect?

In two steps after MoCRA became law on December 29, 2022, according to the Act: the professional-use statement from December 29, 2023, and the adverse event contact on labels from December 29, 2024.1

Has FDA issued the MoCRA fragrance allergen labeling rule?

Not as of October 2026. FDA lists fragrance allergen labeling among the regulations MoCRA requires it to establish, and its MoCRA page, last updated August 10, 2026, points to no proposed rule.2

Is MoCRA labeling the same as the Fair Packaging and Labeling Act?

They work together. FDA describes the FD&C Act and the Fair Packaging and Labeling Act as both requiring cosmetic firms to disclose information on their labels, and MoCRA added new items on top.3

About Arbitr
What does Arbitr check?

Arbitr checks your content against the rules, claims and terms your team has approved, and reports where something doesn't match, by channel, market and language. It reports matches against your rules, not legal verdicts. What to do with each one stays with your team.