What’s the Difference Between Food and Dietary Supplement Labeling in the United States and Canada? What’s the Difference Between Food and Supplement Labeling in the United States and Canada? Food and supplement companies must follow the labeling requirements in each jurisdiction they intend to sell their products in the U.S. and Canada. However, there […]
California Cosmetics Allergens Labeling Requirements Do Businesses Have to List Allergens on Cosmetic Labels? An estimated 10% of people experience allergy-related irritation or hypersensitivity from cosmetic products. The severity of allergic reactions can range from mild dermatitis to anaphylaxis, a potentially life-threatening reaction. Of course, allergens are always a concern with any consumer product, but
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Dietary Supplement Labeling Guide: Understanding Claims, Labels and Regulations Dietary supplements are in high demand, and businesses offering or planning to offer any of the following will need to meet the strict claim, FDA label requirements for dietary supplements: Botanicals Herbs Minerals Protein bars Other supplements Health and nutrition are big business, and while
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Navigating Change: Key Updates in Natural Health Product Labelling Regulations On July 6th, 2022, Health Canada introduced pioneering labeling requirements under the Natural Health Products Regulations (NHPR). It is a groundbreaking labeling initiative, in alignment with the Self-Care framework, that aims to empower consumers in making well-informed decisions about self-care products. These regulations not
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US FDA OTC Monograph User Fee for FY 2022 The US Food and Drug Administration (FDA) announced new Over-the-Counter (OTC) Monograph consumer fees for fiscal year (FY) 2022. The OTC Monograph User Fee Program (OMUFA), which was created by the passage of the March 2020 CARES Act, would require covered OTC drug facilities to
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