FDA warns public vs fake beauty products, face masks
Robie de Guzman • May 28, 2019 • 2642
MANILA, Philippines – The Food and Drug Administration (FDA) on Tuesday warned the public against the purchase and use of the counterfeit versions of some local and international beauty products.
On its Facebook page, the FDA posted a series of advisories against the counterfeit versions of the following products:
3W Clinic’s Fresh Lemon and Fresh Aloe Mask Sheet
RDL babyface Whitening Night Cream 5 in 1
RDL Face-off Fade-out Cream Day Cream
Maybelline New York The Magnum Volum’ Express Waterproof Mascara
M·N® Menow Generation-II Long Lasting Lip Gloss (Variant 34)
The FDA said the mentioned cosmetic products have been verified to be counterfeit, with the help of the brands’ respective distributors, retailers and traders.
The agency warned that fake products pose potential health hazards since these did not go through the required safety assessment and verification process.
The use of substandard and possibly adulterated beauty products, the FDA said, may result in adverse reactions including but not limited to skin irritation, itchiness, anaphylactic shock, and organ failure.
The FDA warned establishments not to distribute the said products as “regulatory actions and sanctions shall be strictly pursued.”
The agency likewise advised the public to be vigilant against cosmetic products that might not be duly notified with the FDA.
Before purchase, consumers may check if a beauty product has been notified with the FDA by searching about the item on their website.
MANILA, Philippines – At least three government agencies are in the list of “priority” agencies of Anti-Red Tape Authority (ARTA) that need their immediate attention due to red tape.
ARTA director-general Jeremiah Belgica said the agencies they are setting their sights on are the Land Transportation Franchising and Regulatory Board (LTFRB), the Food and Drug Administration (FDA) and the Land Registration Authority (LRA).
Belgica said these offices are being focused on due to complaints, investigation results and confidential information.
He added that these agencies need reforms to make their transactions faster and less tedious.
“Nakita talaga natin na they really need to shape up because there’s really red tape inside these agencies,” he told reporters in an economic briefing Wednesday.
However, Belgica clarified that they are yet to thoroughly probe other agencies for red tape, adding that the body has only been investigating for over three months.
ARTA was created through Republic Act 11032, which was signed in May 2018.
It is mandated to ensure effective implementation of the law which is intended to remove red tape in government agencies and ensure the delivery of efficient services.
He also warned other agencies to implement needed reforms because some of them could be worse than the LTFRB, the FDA and the LRA.
“If we would say na they’re the most, marami pa ho kasing mga agencies na hindi pa natin na-thoroughly investigate,” Belgica said.
Meanwhile, ARTA revealed it is set to file a case before the Office of the Ombudsman against a provincial governor on Thursday for allegedly violating the Ease of Doing Business Act or the law that aims for optimal government transactions.
Belgica said the official was accused of delaying the release and processing of permits for some unknown personal reasons.
He, however, refused to divulge any more details including the name of the governor.
The ARTA chief said that since he assumed office in July this year, the agency has already filed cases against seven errant government employees and officials.
Belgica added they are also planning to conduct a weekly filing of cases against government officials who defy the administration’s order to deliver efficient government service and promote ease of doing business.
Belgica said violators of the Anti-Red Tape Act and Ease of Doing Business Act may face penalties as provided for in the law.
On the first offense, violators may face six months suspension while the second offense may mete out dismissal from service, permanent disqualification from holding public office, imprisonment of one up to six years and a fine of P500,000 up to P1 million. – RRD (with details from Rosalie Coz)
MANILA, Philippines – Regulations on processed meat such as well-loved Filipino delicacies tocino and longganisa should be tightened by the Food and Drug Administration (FDA), according to the Department of Agriculture (DA).
According to Agriculture Undersecretary for Consumer Affairs Ernesto Gonzales, consumers cannot be complacent on buying these processed products especially if they are not sure of the source or origin of the raw meat.
Gonzales added that it is difficult to determine if the pork meat is contaminated with African Swine Fever (ASF) once it is processed.
He added that even ‘botcha’ or double-dead pork meat can be made into meat delicacies without the consumer noticing it because of colorings and extenders used in the process.
The official said the best way to determine if the pork meat is safe for consumption is to know the source of the raw meat, and if it is certified by the National Meat Inspection Service (NMIS).
“Kapag na-issue-han na ang karne from slaughterhouse ng meat inspection certificate (once meat from the slaughterhouse is issued with meat inspection certificate), definitely that meat is safe to eat,” Gonzales said.
However, the DA admitted that the government is lacking when it comes to regulations on processed meat so the coordination of the local government units (LGUs) is of utmost importance.
“Iyang problema natin yung mga maliliit na food processors na gumagawa ng mga longanisa, tocino, ang regulation hindi ganoon ka-strict ( The problem with small-time food processors or makers of longanisa and tocino is that the regulation is not that strict), ” Gonzales noted.
If ever the processed meat is infected with ASF, Gonzales said, it is still safe to eat, provided that it went through the proper cooking procedure of 30 minutes under 70’C temperature. – MNP (with details from Rey Pelayo)
DIZON’S FARMS FRESH HABIT COMLD PRESSED JUICE – JUST BEAT IT
LEMON GRASS ICED TEA
The FDA has warned establishments against selling these products.
“All concerned establishments are warned not to distribute violative food products until they have been issued the appropriate authorization, a License to Operate (LTO) for the establishment, and a CPR for the food products,” according to the FDA.
They also advised the public to always check if a food product or food supplement is registered with the FDA through their website (www.fda.gov.ph).—AAC
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