IV.a · Legal notes
iv.
Regulatory and legal notes
Swiss Vitalis CBD is included in ANVISA's published reference of products eligible for the individual personal-import procedure under RDC 660/2022 (Nota Técnica nº 19/2026, Annex I).
Inclusion in ANVISA's reference does not constitute ANVISA registration, commercial authorization, or approval. ANVISA expressly states that listed products have not had their efficacy, quality or safety evaluated, and that they may not be imported, stored, distributed, or resold by legal entities in Brazil.
Swiss Vitalis products are manufactured and sold in the United States. No representation is made that any product is registered, approved, or authorized by ANVISA, the FDA, or any other regulatory authority for the treatment, diagnosis, cure, or prevention of any disease.
Swiss Vitalis LLC (Delaware, USA) is the manufacturer of the product; Novus Byzantium LLC (Wyoming, USA) is the authorized U.S. distributor that handles outbound fulfillment to international personal-import patients. Neither entity is registered with ANVISA, and neither entity operates commercially in Brazil.
Any import of our products into Brazil by an individual patient is the sole responsibility of that patient and must comply with Brazilian law, including RDC 660/2022 and any applicable ANVISA requirements.
Swiss Vitalis does not solicit sales, maintain distributors, or advertise to the Brazilian public. Inquiries from international patients are answered on an informational basis only.