Running an online skin care business is stressful. Isn’t it? or Is it easy to start? I mean various questions also wandering in your mind like what about a skincare license for selling skin care products.? So, here In this article, “do you need a license to sell skin care products ” then you’ll find the best answers for all your questions.
Looking flawless does not happen overnight, it requires dedicated skin routines according to your skin type. Good skincare products help you in alleviating various skin woes like dark circles, and aging, and leave behind a confident and radiant you. Looking at the other side of the coin, usage of some cosmetic product sometime leads to serious side effects like loss of hair, rashes, and even severe cases that may lead to cancer.
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In this post we will also cover skin care products to sell from home or how can you sell skin care products from home.
With a wide array of skin care products readily available in the market, it becomes important to keep a close check on the credibility and side effects of the products. The Food and Drug Administration is the federal agency that regulates cosmetics or skincare products under the FD&C act. In order to understand the control of the FDA over the manufacturing and marketing of cosmetics products, we will discuss some major rules and regulations of the FDA and their possible implications.
- According to the FD&C act, a product is labeled as cosmetics if it is meant for cleansing, improving appearances, or for external beautification. But if the product is meant for disease cure or prevention, or for altering the anatomy and functioning of the body it is labeled as a drug.
- This act prohibits the manufacturing and marketing of adulterated and wrongly-labeled products. The product should not have any damaging side effects and the labeling of the product should be true to the actual effect of the product. The ingredient of the product should be mentioned in accordance with the Fair Packaging and Labelling Act.
- The act does not require any approval of cosmetic products or ingredients except the color additives by the FDA. Other than the color additives and FDA-prohibited ingredients, manufacturers can use any ingredient that is safe to use and maintains the unadulterated quality of the product.
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- FDA holds all the people involved in the interstate commerce of the product like the manufacturers, distributors, and retailers accountable for ensuring that the product that they are doing business with is not adulterated and correctly labeled.
- According to the FD&C Act, cosmetics are not subjected to any kind of test approvals. Although FDA does collect samples for inspection and research in the situation of complaints or suspected non-compliance of safety standards.
- FDA does not have the power to recall any cosmetics from the market. Only the manufacturer has the authority to recall a product but the FDA can request a recall if the product is found to be harmful or adulterated.
- FDA is capable of taking strict actions against people involved in manufacturing or marketing any product that is not in compliance with the law. FDA might completely remove the product from the market or might seize the product. In extreme cases, FDA can file criminal charges against the person responsible.
- FDA also controls the quality of imported products to the USA, working with the U.S Customs and Border Protection (CBP). Imported products can be refused entry if they fail to follow the standards in an examination by the CBP.
- It is not required of any cosmetic company to register, share their product formulation, or get an FDA license for selling their products. Although, it is advisable to voluntarily register under the FDA’s Voluntary Cosmetic Registration Program (VCRP). It should be noted that registering under VCRP by no means depicts FDA approval.
By closely inspecting the above-mentioned rules imposed by FDA regarding running skin care businesses and skin care licenses. We conclude that the FDA does not issue any specific license in regards to selling skincare products. But, it is required by the manufacturers to use ingredients that maintain specific quality standards and to label the product in a non-deceptive way. FDA focuses on the prevention of selling any adulterated products in the market. FDA does not provide guidelines for any specific testing but performs various quality checks like toxicological testing and microbiological testing. It would not only improve the chances of the product being unadulterated but also result in increased credibility of the product.