Genato, Charles Ronald K.

BSP3B-1

M3: Check-in Activity 1

Adulterated Cosmetic Product (International)

Product Name: Puteri Ratu Treatment Cream

Manufactured by Local Company Responsible for Placing the Product in
the Market: NOT INDICATED
Country of Manufacture: Malaysia
Lot/Batch No.: Not Indicated
Manufacturing Date: Not Indicated
Expiration Date: Not Indicated

RA3720 Section and Provision Violation:

CHAPTER X. – Cosmetics
ADULTERATED COSMETICS

SECTION 23. A cosmetic shall be deemed to be adulterated:

(a) if it bears or contains any poisonous or deleterious substance which may render it
injurious to users under the conditions of use prescribed in the labeling thereof, or
under the conditions of use as are customary as usual: Provided, that this provision shall
not apply to coal-tar hair dye, the label of which bears the following legend
conspicuously displayed thereon: "Caution: This product contains ingredients which may
cause skin irritation on certain individuals and a preliminary test according to
accompanying directions should first be made. This product must not be used for dyeing
the eyelashes or eyebrows; to do so may cause blindness", and the labeling of which
bears adequate directions for such preliminary testing. For the purposes of this
paragraph (e) the term "hair dye" shall not include eyelash dyes or eyebrow dyes.

Source:
Food and Drug Administration Philippines. (2022, June 30). FDA Advisory No.2022-1100 || Public Health
Warning Against the Purchase and Use of Adulterated Cosmetic Product FLASHH SKINZZ NIGHT CREAM
as Reported in the ASEAN Post-Marketing Alert System (PMAS) - Food and Drug Administration. Food
and Drug Administration -. https://www.fda.gov.ph/fda-advisory-no-2022-1100-public-health-warning-
against-the-purchase-and-use-of-adulterated-cosmetic-product-flashh-skinzz-night-cream-as-reported-
in-the-asean-post-marketing-alert-system-pmas/
Misbranded Medical Device (International)

Product Name: “GREENS POWER DISPOSABLE SURGICAL MASK (IN FOREIGN CHARACTERS)”

RA 3720 Section and Provision Violation:

MISBRANDED DRUGS AND DEVICES

SECTION 19. A drug or device shall be deemed to be misbranded:

(c) if any word, statement, or other information required by or under authority of this
Act to appear on the label or labeling is not prominently placed thereon with such
conspicuousness (as compared with other words, statements, designs, or devices, in the
labeling) and in such terms as to render it likely to be read and understood by the
ordinary individual under customary conditions of purchase and use.

Source:
Food and Drug Administration Philippines. (2022, April 12). FDA Advisory No.2022-0908 || Public Health
Warning Against the Purchase and Use of the Following Misbranded Medical Device Product “GREENS
POWER DISPOSABLE SURGICAL MASK (IN FOREIGN CHARACTERS).” Https://Www.Fda.Gov.Ph. Retrieved
July 13, 2022, from https://www.fda.gov.ph/fda-advisory-no-2022-0908-public-health-warning-against-
the-purchase-and-use-of-the-following-misbranded-medical-device-product-greens-power-disposable-
surgical-mask-in-foreign-characters/