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Developing targeted solutions for skin health requires some basic knowledge of formulary and regulatory standards.
August 15, 2018
By: Sean Moloughney
Editor, Nutraceuticals World
Formulating skin care products requires a cross-disciplinary knowledge base that is hard to obtain and master. It can be a daunting, time-consuming, and costly process when skin care product formulas fail or run into legal issues. This article provides a useful and easy to understand primer on legal language as well as essential tips on how to formulate an effective, safe, and legal skin care product. Regulation Guidelines First, it’s critical to be well-informed on the legalities of formulating skin care products. Cosmetic products and ingredients, other than color additives, do not require pre-market approval by the U.S. FDA. However, laws that apply to cosmetics on the market may vary from state to state (interstate commerce). The two most important laws pertaining to cosmetics marketed in the U.S. are the Federal Food, Drug, and Cosmetic Act (FD&C) and the Fair Packaging and Labeling Act (FPLA). The FD&C defines cosmetics by their intended use as “articles intended to be rubbed, poured, sprinkled, or sprayed on, introduced into, or otherwise applied to the human body … for cleansing, beautifying, promoting attractiveness, or altering the appearance.” The products that fit this definition include perfumes, lipsticks, nail polishes, eye and face makeup, shampoo, hair dyes, and deodorants. Claims It’s very important to be informed about various claims that should be noted for labeling or describing cosmetic products. If the product is intended for a therapeutic use, such as preventing or treating disease, or changes the effects or functionality of the body, then it is considered a drug. Products intended to make individuals more attractive are considered cosmetics. For example, the word “moisturizing” is a cosmetic claim. If the goal of a product is intended to make fine lines and wrinkles to appear less noticeable by moisturizing the skin, then it’s cosmetic. Similarly, “primers” intended to make the signs of aging less noticeable by hiding them is also considered cosmetic. Products that are intended to affect the structure or function of the body, such as the skin, are considered drugs or sometimes medical devices, even if they affect the appearance of skin. For example, if a product is intended to remove wrinkles or increase the production of collagen in the skin, then it is considered a drug or a medical device. Good Manufacturing Practices Good Manufacturing Practices (GMPs) constitute specific guidelines that should be followed when developing skin care products. If a company manufactures skin care products, the risk of misbranding cosmetics or contamination is reduced by following GMP guidelines. Under these guidelines, buildings and facilities used for manufacturing should be of suitable construction, design, size, and maintained in a clean and orderly manner. Equipment used should be of appropriate design, size, and material for the intended purpose in order to prevent contamination. Defective equipment should be removed and suitable tools should be calibrated regularly and checked according to standard operating procedures (SOP) with results documented. Personnel in charge of supervising or manufacturing skin care products should have the required education, experience, and training to perform assigned duties. Personnel should adhere to the necessary protective clothing guidelines when coming in direct contact with cosmetic raw materials, in-process materials, finished products, or contact surfaces. Eating food, drinking beverages, or using tobacco should be restricted to appropriately designated areas, away from processing and storage areas. To ensure raw materials are safe and to fulfill their intended purpose, they should be handled and stored to prevent mistakes (misidentification and selection errors), contamination with chemicals or microorganisms, and degradation from exposure to harsh environmental conditions (cold, heat, moisture, sunlight). Raw materials should be held in closed containers and stored off the floor, labeled with identity, lot number, and control status (quarantine or release). Regular testing will ensure the safety and identification of any contaminants in the sample. Documents Material Safety Data Sheets (MSDS): A document that provides vital information on the potential hazards of a chemical product and how to work safely with the chemical product. It also contains information on the handling, storage, usage, and emergency procedures all related to the hazards of the product. Standard Operating Procedures (SOP): A procedure specific to your operation that describes the activities necessary to complete tasks in accordance with industry laws, regulations, or even standards for running your own business. Any document that is a “how to” falls into the category of procedures. In a manufacturing environment, the most important example of an SOP is the step-by-step product line procedures used to make products as well as train personnel. SOPs are standards and policies needed in the administration, marketing, and operation within a business to ensure success. They can create:
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