The following important message about the safety of temporary tattoos is from the Food and Drug Administration.

Spring break is on the way, or maybe summer vacation. It is time to pack your swim suit, hit the beach, and perhaps indulge in a little harmless fun. What about getting a temporary tattoo to mark the occasion? Who could it hurt to get a temporary tattoo?

It could hurt you, if you actually get one. Temporary tattoos typically last from three days to several weeks, depending on the product used for coloring and the condition of the skin. Unlike permanent tattoos, which are injected into the skin, temporary tattoos marketed as “henna” are applied to the skin’s surface.

However, “just because a tattoo is temporary it doesn’t mean that it is risk free,” says Linda Katz, M.D., M.P.H., director of FDA’s Office of Cosmetics and Colors. Some consumers report reactions that may be severe and long and outlast the temporary tattoos themselves.

MedWatch, FDA’s safety information and adverse event (bad side effects) reporting program, has received reports of serious and long-lasting reactions that consumers had not bargained for after getting temporary tattoos. Reported problems include redness, blisters, raised red weeping lesions, loss of pigmentation, increased sensitivity to sunlight, and even permanent scarring.

Some reactions have led people to seek medical care, including visits to hospital emergency rooms. Reactions may occur immediately after a person gets a temporary tattoo, or even up to two or three weeks later.

Not Necessarily Safe

You may be familiar with henna, a reddish-brown coloring made from a flowering plant that grows in tropical and subtropical regions of Africa and Asia. Since the Bronze Age, people have used dried henna, ground into a paste, to dye skin, hair, fingernails, leather, silk and wool. This decoration—sometimes also known as mehndi—is still used today around the world to decorate the skin in cultural festivals and celebrations.

However, today so-called “black henna” is often used in place of traditional henna. Inks marketed as black henna may be a mix of henna with other ingredients, or may really be hair dye alone. The reason for adding other ingredients is to create tattoos that are darker and longer lasting, but use of black henna is potentially harmful.

That’s because the extra ingredient used to blacken henna is often a coal-tar hair dye containing p-phenylenediamine (PPD), an ingredient that can cause dangerous skin reactions in some people. Sometimes, the artist may use a PPD-containing hair dye alone. Either way, there’s no telling who will be affected. By law, PPD is not permitted in cosmetics intended to be applied to the skin.

You may see “black henna” used in places such as temporary tattoo kiosks at beaches, boardwalks, and other holiday destinations, as well as in some ethnic or specialty shops. While states have jurisdiction over professional practices such as tattooing and cosmetology, that oversight differs from state to state. Some states have laws and regulations for temporary tattooing, while others don’t. So, depending on where you are, it’s possible no one is checking to make sure the artist is following safe practices or even knows what may be harmful to consumers.

A number of consumers have learned the risks the hard way, reporting significant bad reactions shortly after the application of black henna temporary tattoos.

• The parents of a 5-year-old girl reported that she developed severe reddening on her forearm about two weeks after receiving a black henna temporary tattoo. “What we thought would be a little harmless fun ended up becoming more like a nightmare for us,” the father says. “My hope is that by telling people about our experience, I can help prevent this from happening to some other unsuspecting kids and parents.”
• The mother of a 17-year-old girl agrees. “At first I was a little upset she got the tattoo without telling me,” she says. “But when it became red and itchy and later began to blister and the blisters filled with fluid, I was beside myself.” She explains that as a nurse, she’s used to seeing all manner of injuries, “but when it’s your own child, it’s pretty scary,” she says.
• And another mother, whose teenager had no reaction to red henna tattoos, describes the skin on her daughter’s back as looking “the way a burn victim looks, all blistered and raw” after a black henna tattoo was applied there. She says that according to her daughter’s doctor, the teenager will have scarring for life.

If you have a reaction to or concern about a temporary tattoo or any other cosmetic, in addition to recommending that you contact your health care professional, FDA asks you to contact MedWatch, the agency’s problem-reporting program. You can also call 1-800-FDA-1088 to report by telephone, or contact the nearest FDA consumer complaint coordinator in your area or a problem with tattoos.

Before you apply your makeup or use that personal care item, ask yourself what what chemicals are in what you are using on your face and how safe are they?

You are doing so much to safeguard your health …eating well and getting regular exercise, but are you unknowingly adding chemicals to your body through your makeup and personal care items?

According to the Environmental Work Group (EWG), a nonprofit organization that uses public information to protect public health and the environment, the US government has no authority to require companies to test personal care products for safety before they reach the store shelf.

EWG’s research documents that 22 percent of all personal care products may contain the cancer-causing contaminant 1,4-Dioxane, and more than half of all sunscreens contain oxybenzone, a potential hormone disruptor. Other studies raise serious concerns about makeup such as lead in lipsticks and chemicals in fragrance and artificial preservatives in personal care products.

Fragrance, in particular, has become a source of concern due to the unlisted ingredients behind the scents. A study of 17 popular fragrances by the Environmental Working Group and the Campaign for Safe Cosmetics, advocacy groups focused on exposing products they deem hazardous to health, found 14 undisclosed chemicals, on average. Among them were phthalates, which are used to soften plastic and have been linked to various ailments.

The following groups of chemicals are currently being studied for links to breast cancer:

• Parabens – chemicals commonly used as preservatives in many cosmetic products, including makeup, moisturizers, hair care products, and gels.

• Phthalates – used to hold color and reduce brittleness in nail polish and hair spray. They’re also found in many personal care items.

Before you use your current makeup again, or buy a new makeup, visit the Environmental Working Group’s (EWG) Skin Deep site and  check your makeup and personal care items scores.  EWG lists a product’s hazard score based on the chemicals links to cancer, allergies, and other issues.

September is National Food Safety Education Month and consumers need to know that myths about keeping food safe in the refrigerator aren’t true.

Myth 1: I know my refrigerator is cold enough – I can feel it when I open it! Anyway, I have a dial to adjust the temperature.

Fact:  Unless you have thermometers built into your fingers, you need to use a thermometer to ensure your refrigerator is at or below 40 °F.  And that dial? Important, but it is not a thermometer.

As many as 43% of home refrigerators have been found to be at temperatures above 40 °F, putting them in the food safety “danger zone” where harmful bacteria can multiply and make you and your family sick!

Slow the growth of bacteria by using a refrigerator thermometer to tell if your refrigerator is at 40 °F or below. And if it isn’t?  Use that dial to adjust the temperature so it will be colder. Then, use your refrigerator thermometer to measure again.

Myth 2:  Cross-contamination doesn’t happen in the refrigerator – it’s too cold in there for germs to survive!

Fact:  Bacteria can survive and some even grow in cool, moist environments like the refrigerator.

In fact, Listeria bacteria can grow at temperatures below 40 °F! A recent study showed the refrigerator produce compartment was one of the “germiest” places in the kitchen, containing Salmonella and Listeria.

To reduce the risk of cross-contamination in your refrigerator:

• Keep fresh fruits and vegetables separate from raw meat, poultry, seafood, and eggs
• Clean up food and beverage spills immediately, and
• Clean your refrigerator regularly with hot water and liquid soap.  Don’t forget to clean the refrigerator walls and undersides of shelves!

Myth 3: I left some food out all day, but if I put it in the refrigerator  now, the bacteria will die.

Fact:   Refrigerator temperatures can slow the growth of bacteria, but will not stop the growth of bacteria in food. 

If food is left out at room temperature for more than two hours, putting it into the refrigerator will only slow bacterial growth, not kill it. Protect your family by following the 2-hour rule—refrigerate or freeze meat, poultry, seafood, eggs, cut fresh fruits and vegetables, and all cooked leftovers within 2 hours of cooking or purchasing. Refrigerate within 1 hour if the temperature is above 90 ºF.

While refrigeration does slow bacterial growth, most perishables will only keep for a few days in the refrigerator. To keep perishables longer than a few days—like most meat, poultry and seafood—you can freeze them.

Myth 4:  I don’t need to clean my refrigerator produce bin because I only put fruit and vegetables in there.

FACT:   Naturally occurring bacteria in fresh fruits and vegetables can cause cross-contamination in your refrigerator.

A recent NSF International study found that the refrigerator produce compartment was the #1 “germiest” area in consumers’ kitchens!  To prevent the buildup of bacteria that can cause food poisoning, it is essential to clean your produce bin and other bins in your refrigerator often with hot water and liquid soap, rinse thoroughly, and dry with a clean cloth towel or allow to air dry outside of the refrigerator.

For more myths and facts about food safety, go to:
www.fightbac.org/food-safety-education/home-food-safety-mythbusters/

In an effort to quit,many people who smoke, are turning to e-cigarettes to help ease the process of giving up cigarettes entirely. Adolescents are experimenting with e-cigarettes. Yet little is known about the long term effects of using e-cigarettes.

What follows is a press release that speaks to the concerns of The  American Association for Cancer Research (AACR) and the American Society of Clinical Oncology (ASCO) with regard to e-cigarettes.

 Press release... The American Association for Cancer Research (AACR) and the American Society of Clinical Oncology (ASCO), in a joint letter responding to a proposal by the U.S. Food and Drug Administration (FDA) to extend its regulatory authority over tobacco products, today urged the agency to regulate electronic cigarettes (e-cigarettes), cigars, and all other tobacco products and to strengthen the proposed regulations for newly deemed products.

“There is no safe form of tobacco use,” said Margaret Foti, PhD, MD (hc), chief executive officer of the AACR. “Tobacco is the leading cause of preventable deaths in the United States, and among its dire health consequences are 18 different types of cancer. It is imperative that the FDA takes action to regulate all tobacco products. The future health of the American people, in particular our nation’s children, depends on it.”

The AACR and ASCO applauded the FDA’s proposal to regulate e-cigarettes. “We believe it is vitally important for the FDA to begin regulating these products,especially because we don’t know much about the health effects of e-cigarette use. We are also quite concerned that e-cigarettes may increase the likelihood that nonsmokers or former smokers will use combustible tobacco products or that they will discourage smokers from quitting,” said Peter P. Yu, MD, FASCO, president of ASCO.

“There are insufficient data on the long-term health consequences of e-cigarettes, their value as tobacco cessation aids, or their effects on the use of conventional cigarettes. Any benefits of e-cigarettes are most likely to be realized in a regulated environment in which appropriate safeguards can be implemented,” said Roy S. Herbst, MD, PhD, chair of the AACR Tobacco and Cancer Subcommittee and chief of medical oncology at Yale Comprehensive Cancer Center.

The AACR and ASCO support many of the FDA’s proposals for regulating e-cigarettes and other products, but urge the agency to do more. Specifically, preventing children from using tobacco products is crucial and can be achieved by efforts such as banning youth-oriented advertising and marketing, self -service product displays, and tobacco company sponsorship of youth-oriented events, in addition to restricting sales to minors and implementing age-verification procedures for internet sales.

Expressing grave concern about the proliferation of flavored e-cigarettes, the AACR and ASCO encouraged the agency to ban e-cigarette flavors or flavor names that are brand names of candy, cookies, soda, and other such products, and to prohibit e-cigarettes containing candy and other youth-friendly flavors, unless there is evidence demonstrating that they do not encourage young people to use these products.

The AACR and ASCO strongly discouraged the FDA from exempting “premium” cigars from regulation, an option the agency is considering. “All cigars pose serious health risks,” said Graham Warren, MD, PhD, chair of ASCO’s Tobacco Cessation and Control Subcommittee. “As the FDA itself noted in the proposed rule, even cigar smokers who do not inhale have a seven to 10 times higher overall risk of mouth and throat cancer compared with individuals who have never smoked.Exempting these dangerous products from FDA regulation is clearly not in the best interest of public health.”

Noting that both large and small cigars are of increasing interest to youth and adult users, the AACR and ASCO underscored that the continued availability of premium cigars in an unregulated market, compounded with the ability of the tobacco industry to strategically market its products to youths and young adults, could reverse the progress made in reducing youth tobacco use.

Finally, the AACR and ASCO urged the FDA to drop the “consumer surplus” discount used to assess the net impact of the proposed deeming rule. This discount allows the FDA to only consider 30 percent of the benefits achieved via tobacco cessation due to the costs associated with this proposed regulation, including the “lost pleasure” of smoking. The AACR and ASCO stressed that addiction is an unwelcome burden for many tobacco users and that many consumers are not making rational and fully informed choices when initiating and continuing their use of tobacco products.

The FDA wants you to be aware of the growing problem of Antibiotic Resistance. The following information comes directly from the FDA literature on the subject.

Antibiotic drugs can save lives. But some germs get so strong that they can resist the drugs. The drugs don’t work as well. Germs can even pass on resistance to other germs.

 Antibiotic drugs normally work by killing germs called bacteria, or they stop the bacteria from growing. However,  sometimes not all of them are stopped or killed. The strongest ones are left to grow and spread. A person can get sick again. This time the germs are harder to kill.

The more often a person uses an antibiotic, the more likely it is that the germs will resist it. This can make some diseases very hard to control. It can make you and your children sick longer and require more doctor visits. You may need to take drugs that are even stronger.

 There are Two Main Types of Germs

 Bacteria and viruses are the two main types of germs. They cause most illnesses. Antibiotics can kill bacteria, but they do not work against viruses. Viruses cause:• Colds • Coughs• Sore throats • Flu• Bronchitis • Sinus problems• Ear infections

Bacteria live in drinking water, food, and soil. They live in plants, animals, and people. Most of them do not hurt people. Some even help us to digest food. But other bacteria cause serious diseases such as tuberculosis (TB) and Lyme disease.

 How Does this Affect Me?

 If you have a virus, taking antibiotics is not a good idea. Antibiotics don’t work against viruses. The medicine will not help you. It might even harm you. Each time you take one, you add to the chances that bacteria in your body will be able to resist them. Later that could make you very sick. Finding the right treatment could be a problem.

 What Common Mistakes Do Patients Make?

• Patients ask for antibiotics they don’t need. For example, they ask for antibiotics to treat a cold.

• They don’t take antibiotics the way the doctor says. For example, they stop taking the drug before all the pills are used. That can leave the strongest germs to grow.

• They save antibiotics and take them on their own later

What is the FDA Doing About the Problem?

The FDA wants doctors to be more careful about giving antibiotics when they are not needed.

• The FDA will require new labeling for doctors.

• One of the new labels must say that these drugs should be used only for infections caused by bacteria.

• Another label will ask doctors to explain to their patients the right way to use the drugs.

 What Should I Do?

 • Don’t demand an antibiotic when your doctor says you don’t need it.

• Don’t take an antibiotic for a virus (cold, cough, or flu).

• Take your medicine exactly the way the doctor says. Don’t skip doses.

• Don’t stop taking your medicine when you feel better. Take all the doses.

• Don’t take leftover medicine.

• Don’t take someone else’s medicine.

• Don’t rely on antibacterial products (soaps, detergents, and lotions). There is no proof that these products really help.

We all need to be wary about becoming antibiotic resistant