Pet Supplements or Veterinary Health Products? USA vs Canada

Pet Supplements or Veterinary Health Products? USA vs Canada
Andrew Parshad
President & Founder of Quality Smart Solutions

In This Article:

Pet supplements and veterinary health products comparison between the U.S. and Canada

If you are planning to market animal health products, the question of pet supplements or veterinary health products will come up fast. This difference matters, especially if you’re selling in both the United States and Canada.  

What qualifies as a supplement in the U.S. might be considered a drug or a Veterinary Health Product (VHP) in Canada. Misunderstanding this can lead to product seizures, warning letters, or even a ban from entering the market. 

In this blog, we will walk you through how both countries regulate these products, why it matters for your business, and how to stay compliant across borders. Keep reading to discover the key distinctions and what they mean for your regulatory obligations. 

What are pet supplements in the U.S.? 

In the U.S., pet supplements aren’t officially recognized by the FDA. Instead, they fall under regulations for animal foods or drugs. If your product contains only approved feed ingredients and avoids therapeutic claims, it may be considered food. But if it claims to treat or prevent disease, it’s likely a drug. 

Claims like “supports mobility” may be tolerated, while “relieves joint pain” could require drug approval. You must also meet FDA manufacturing standards and, in many cases, register at the state level with AAFCO. Learn more at the FDA’s Animal & Veterinary Products page. 

What are veterinary health products in Canada? 

Canada classifies pet supplements as Veterinary Health Products (VHPs), which are low-risk products used to maintain or promote animal health, not treat disease. 

To sell a VHP, you must notify Health Canada and use only permitted ingredients. Claims must be non-therapeutic, and your label must match your submission. Bilingual packaging is required. 

This process is more flexible than a drug application but still demands accuracy. For more information, visit Health Canada’s VHP page. 

Comparing U.S. and Canadian regulations 

To help you spot the key differences faster, here’s a side-by-side look at how each system defines and regulates these products: 

Aspect United States Canada 
Regulatory Category Animal food or animal drug Veterinary Health Product (VHP) 
Recognized Term No official recognition of “pet supplements” “Pet supplements” not used; products are VHPs 
Governing Body FDA + state-level (AAFCO involvement) Health Canada 
Ingredient Approval Based on AAFCO listings or approved drug ingredients Must use substances from the VHP permitted substances list 
Claim Restrictions Cannot make disease claims without drug approval Must avoid disease-related claims 
Pre-Market Requirement No federal registration, but state registration may apply VHP Notification required before sale 
Packaging Requirements Varies by state Bilingual packaging required (English and French) 
Enforcement Risk Product seizure or warning letters Border detention or withdrawal from market 

Common mistakes to avoid 

Many companies overlook the fine print that separates a compliant product from one that might be stopped at customs or pulled from shelves. So, here are some of the most common mistakes to watch out for: 

1. Assuming U.S. rules apply in Canada

Some companies try to bring “supplements” into Canada without realizing that these are classified differently. In Canada, the word “supplement” is not typically used for animals. It is either a drug or a VHP. 

2. Making unapproved claims

Whether you are in the U.S. or Canada, therapeutic claims (like “cures skin infections”) can quickly move your product into the drug category, which has stricter requirements. 

3. Skipping notification in Canada

If you do not notify Health Canada before selling your product, it can be detained at the border or removed from store shelves. 

4. Using non-compliant ingredients

Canada has a strict list of permitted substances. Using an unapproved ingredient can delay your product launch or lead to immediate enforcement. 

5. Neglecting state registrations in the U.S.

Some companies overlook that even if their product meets federal guidelines, they still need to register in individual states, each with its own process and fees. 

How to stay compliant 

As you’ve seen, each country has its own approach. Here’s how to stay aligned: 

For the United States: 

  1. Check AAFCO ingredient approval and avoid therapeutic claims. 
  2. Review FDA guidance on marketing language. 
  3. Register with individual states where needed. 

For Canada: 

  1. Submit a VHP notification to Health Canada. 
  2. Use only permitted ingredients and non-therapeutic claims. 
  3. Ensure bilingual packaging and label consistency. 

Frequently asked questions

Can I sell the same pet product in both countries?

Not as-is. A product that is legal in the U.S. might need reformulation, new packaging, or a claim adjustment to comply with Canadian VHP rules. Even the terminology and suggested usage may need to change.

Not always, but you may need different versions of the label and accompanying literature to match local compliance requirements.

No. While there are overlaps in good manufacturing practices and safety expectations, each country has distinct pathways.

Yes. What is considered a functional benefit in the U.S. might be interpreted as a therapeutic claim in Canada. Avoid crossover language that triggers higher scrutiny.

By aligning with regulations in both the U.S. and Canada, your brand can access two of the largest pet-owning populations in North America. Cross-border compliance adds credibility and can give your brand a competitive edge.

Compliance is your competitive edge 

Navigating pet product regulations across borders takes more than good intentions. It requires precision, up-to-date knowledge, and a clear strategy tailored to each market. 

Whether you’re launching a new product or adapting an existing one, our team can help you stay compliant, save time, and avoid costly setbacks. We monitor updates from both the FDA and Health Canada,so you don’t have to. 

Need help getting started? Contact us today to ensure your products meet regulatory standards in the U.S. and Canada. 

0/5 (0 Reviews)
Picture of Andrew Parshad
Andrew Parshad
Andrew Parshad is President, CEO and founder of Quality Smart Solutions, a North American compliance solutions provider offering regulatory and quality assurance services to comply with FDA & Health Canada brands and ingredients regulations in the categories of dietary supplements, foods, cosmetics, OTC drugs and medical devices. Andrew started Quality Smart Solutions in 2007. Since that time he and his firm has served thousands of clients worldwide . Andrew's affiliate company, Quality IMPORT Solutions that offers import agent services into the Canadian market as a government licensed importer for foods, dietary supplements and medical devices.
Follow the expert:
Related Articles

Subscribe to global regulatory updates

We use cookies to display personalized content, analyze site traffic, provide recommendations, and ensure you have a great browsing experience. By continuing to use our site, you consent to our use of cookies. Privacy Policy.