Nada Question For Note 1 And 2 Flashcards
intended to be rubbed, poured, sprinkled, sprayed on, introduced into, or otherwise applied to the human body for cleansing, beautifying, promoting attractiveness, or altering the appearance without affecting the body’s structure or function.
L
influence the biological function of the skin.
.
fastest-growing segment of the natural personal care industry.
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testing to determine whether beneficial ingredients actually live up to a manufacturer’s claims is not mandatory.
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not subject to review by the Food and Drug Administration (FDA).
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manufacturer may not claim that these products penetrate beyond the skin’s surface layers or that they have drug like or therapeutic effects.
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no division between active ingredients and other ingredients is required; they are all listed together.
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became a controversial nationalistic issue in which a product or ingredient was safe for distribution in one location but not in another.
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To date, there is no agreement on the following :
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Establishment of an agency with worldwide responsibility for the safety of ingredients and of their blends (finished products).
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Agreement between countries or legislative units enforcing such rules globally and their modifications whenever newly developed information should require this.
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Whether a product falls under the Food and Drug Administration’s (FDA) jurisdiction (control) as cosmetic product depends largely
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To determine a product’s intended use, the FDA relies on the
.
Any enforcement actions against an adulterated or misbranded cosmetic product can by necessity be taken
.
are misleading if they fail to bear all the information required under the FDCA.
.
result from insufficient information for the consumer, for an improperly formed or filled container.
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The FDA’s primary discovery tool is the
.
FDA also investigates
.
may bring a criminal suit against the company and its officials.
.
FDA regulations require products whose safety has not been confirmed to bear a .
.
PROHIBITED AND HAZARDOUS SUBSTANCES
.
Bithionol
.
hexachlorophene
.
mercury
.
vinyl chloride (
.
chloroform
.
methylene chloride
.
chlorofluorocarbon
.
nitrosoamine
.
Cosmetics that contain color additives not covered by a regulation are
.
All foreign (that is, non- U.S.) drug manufacturing establishments should
.
does not inspect the production facilities of foreign OTC drug makers for compliance with current Good Manufacturing Practices (GMPs).
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The primary purpose of ingredient labeling is the need to
.
The FDA regulations permit three different formats for the ingredient declaration:
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Warning statements are required by regulation for
.
Warning statements must be
.
lot and batch codes are commonly added to the cosmetic product labeling to
.
that a cosmetic product represented for nonprescription, over the counter (OTC) drug, purposes will be held to the applicable OTC drug standard.
.
The top most layer of skin,
.
contains melanocytes,
cells produce a pigment called melanin.
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from the squamous layer
are pushed up through two thin epidermal
layers; the stratum granulosum and the strat.
lucidum
.
the outermost visible
layer of the epidermis.
;
made up of 10 to 30 thin layers of these dead
cells.
.
takes nearly a month
for the…….. to be completely
replaced.
.
nuclei of the cells in the epidermis
and the collagen of the dermis.
.
In normal epidermis, the water content gets
less
.