Standardized service
Pet Treats Label Review (AAFCO/FDA)
U.S. pet food labels must satisfy both FDA federal rules and state requirements generally based on the AAFCO model regulations. We check every mandatory element of your label, deliver an action-point report and a suggested draft, and reduce the risk of detention and warning letters.
On this page
What this service is
At the federal level, pet food labeling is governed by the adulteration and misbranding provisions of the Federal Food, Drug, and Cosmetic Act, administered by FDA's Center for Veterinary Medicine (CVM). At the state level, most states adopt the AAFCO model pet food regulations, which set specific requirements for product names, guaranteed analysis, and nutritional adequacy statements.
FDA does not approve labels before marketing; it samples products once they are on the market. Non-compliant labels lead to detentions and publicly posted warning letters, so a third-party label review before launch is standard risk control.
Who needs it
Prerequisites and sequence
- Provide the final (or near-final) label artwork; a Word text version is acceptable if no artwork exists.
- Have the full formula, target species, and life stage defined.
- If the product contains animal-origin ingredients, confirm whether a USDA APHIS import permit is needed in parallel — label review and permits do not replace each other.
Who holds regulatory responsibility
Label compliance rests with the manufacturer or distributor named on the label. We provide third-party review findings and correction recommendations; you confirm and adopt the final label.
Materials we need from you
Process
- 01
Check identity elements: product name, intended species, net quantity
- 02
Review ingredient statement ordering and ingredient naming
- 03
Verify the guaranteed analysis and nutritional adequacy statement
- 04
Review feeding directions, responsible-party naming, and country-of-origin marking
- 05
Issue an action-point report with corrections marked on the existing label
- 06
Provide a suggested draft label and re-review your revised version
Deliverables
Timeline
The initial review takes about two weeks; each re-review of a revised label takes a minimum of three business days. Overall timing depends on how quickly corrections are implemented.
Scope
What we provide
- Element-by-element check of mandatory label information
- Ingredient naming and claims compliance assessment
- Action-point report and suggested draft label
- Re-review of the corrected label
What is not included
- Graphic design and artwork production
- Laboratory testing behind the guaranteed analysis (can be arranged separately)
- State feed registration or tonnage reporting obligations (assessed separately where applicable)
What usually follows
Common pitfalls
Pricing
Pricing depends on your product, quantity, and target market. Submit your product details and we will come back with a defined scope and quote.
FAQ
Does FDA approve my label in advance?
No. FDA does not pre-approve labels; it verifies them on a sampling basis after products reach the market. Non-compliance results in detention or warning letters published on FDA's website — which is why a pre-launch third-party review matters.
Is a guaranteed analysis mandatory?
Under the AAFCO model regulations adopted by most states, pet food labels must carry a guaranteed analysis (e.g., minimum crude protein and crude fat, maximum crude fiber and moisture). The exact elements vary by product type and are confirmed during the review.
Can a review guarantee FDA clearance?
No one can offer a hundred-percent guarantee given the nature of regulatory compliance. A systematic check against the mandatory requirements substantially reduces the risk of detention and warning letters.
Can you review text copy without artwork?
Yes. A Word file is sufficient — we identify all mandatory information and provide a suggested draft. Graphic production still needs to be done by your designer.
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Disclaimer
This is a third-party label review and does not constitute FDA endorsement or legal advice. Compliance responsibility rests with the manufacturer/distributor named on the label.