Henna tattoos pose danger, FDA warns

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Henna tattoos pose danger, FDA warns

Henna tattoos pose danger, FDA warns
The Food and Drug Administration (FDA) warned on Tuesday públicocontra the adverse reaction of the skin produced by staining of the skin temporalproductos cosmetics, including henna tattoos.

In a warning, the FDA said the public may be risking permanent scars get if they go for henna tattoos that have uncertain ingredients.

"This is the additional ingredients that are potentially harmful, especially if they are of hair dye coal tar containing p-phenylenediamine (PPD)," the FDA said.

He explained that the PPD causes adverse skin reactions, which may lead to severe inflammation and scarring.

"There is no way to know if the PPD is mixed in henna preparations unless they are properly labeled according to the standard of the Philippines," lala FDA also said.

Henna danger Because of this, the health agency advised the public to always go for henna tattoos that are FDA approved.

He explained that this is because all temporary skin coloring products, commonly known as henna dye, need the approval of the FDA comoproductos cosmetics before they are marketed or used in the country.

"Consumers are advised to ask the marketing authorization by the FDA or cosméticaantes receiving notice of a temporary tattoo," the FDA said.

The FDA advisory came after a five year old in the United Unidosenrojecimiento developed severe swelling of the skin, where the hennatatuaje was placed.

However, in the Philippines, the FDA said it has not received any similar complaints.

"Consumers who experienced adverse reactions were requested to send its report [email protected] ," the FDA said.

On the other hand, the dye henna tattoo manufactures, importers, distributors traders OSE highly recommended to apply for a license to operate andthe marketing authorization from the FDA.

The FDA said the lack of registration is a direct violation of RepúblicaLey 3720 or the Federal Food, Drug, and Cosmetic, and as the Republic Act 9711 or the Law of the FDA 2009. (HDT / Sunnex)

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