FIPP Law Review 2024/2025 Exam
Questions with Detailed Verified
Answers (100% Correct Answers) |
Already Graded A+
what did the Pure Food and Drug act of 1906 do? - 🧠ANSWER
✔✔prohibited interstate sale of adulterated and misbranded food and drugs
and addresses some product labeling issues
what were the product labeling issues addressed in the pure food and drug
act? - 🧠ANSWER ✔✔-labels cannot be false or misleading about
ingredients
-no requirement to disclose ingredients
-11 dangerous ingredients were identified but could be used as long as
listed (cocaine, heroine, ect)
what did the pure food and drug act of 1906 lead to? - 🧠ANSWER ✔✔the
creation of the modern day food and drug administration (FDA)
COPYRIGHT©PROFFKERRYMARTIN 2025/2026. YEAR PUBLISHED 2025. COMPANY REGISTRATION NUMBER: 619652435. TERMS OF USE.
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PRIVACY STATEMENT. ALL RIGHTS RESERVED
,what is the Sulfanilamide tragedy of 1937? - 🧠ANSWER ✔✔-Tennessee
drug company marketed "Elixir Sulfanilamide" as a wonder drug for
ailments from gonorrhea to sore throats
-dug contained chemical analog of antifreeze "diethyl glycol"
-killed over 105 people (adults and children) which created a public outcry
-failure to list ingredients or test the safety of those ingredients was not a
violation of the 1906 pure food and drug act
What did the sulfanilamide tragedy lead to? - 🧠ANSWER ✔✔giving
enforcement authority to the federal food, drug, and cosmetic act of 1938
what was the Federal food, drug, and cosmetic act of 1938? - 🧠ANSWER
✔✔set of laws passed by congress in 1938 which gave authority to the US
food and drug administration to oversee the safety of food, drugs, and
cosmetics
what were the FD&C requirements that came from the federal food, drug,
and cosmetic act of 1938? - 🧠ANSWER ✔✔-drug labels must include
directions for safe use
-required pre-market approval for new drugs to ensure safety
-prohibited false therapeutic claims for drugs
COPYRIGHT©PROFFKERRYMARTIN 2025/2026. YEAR PUBLISHED 2025. COMPANY REGISTRATION NUMBER: 619652435. TERMS OF USE.
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PRIVACY STATEMENT. ALL RIGHTS RESERVED
, -authorized factory inspections
-FDA given regulatory authority over medical devices and cosmetics for the
first time
adulteration definition? - 🧠ANSWER ✔✔-contains any poisonous or
deleterious substance which may render it injuries to uses when used as
directed
-contains any filthy, putrid, or decomposed substance (ie expired drugs)
-prepared, packaged, or held under unsanitary conditions and became
contaminated or rendered injuries
-has a poisonous or deleterious container
-contains an unapproved food or color additive
misbranded definition? - 🧠ANSWER ✔✔-incorrect drug, patient name,
prescriber name, or directions
-is missing poison prevention ot tamper-resistant packaging
-OTC products without "adequate directions for use"
-prescription package/products without "adequate directions for use"
COPYRIGHT©PROFFKERRYMARTIN 2025/2026. YEAR PUBLISHED 2025. COMPANY REGISTRATION NUMBER: 619652435. TERMS OF USE.
3
PRIVACY STATEMENT. ALL RIGHTS RESERVED
Questions with Detailed Verified
Answers (100% Correct Answers) |
Already Graded A+
what did the Pure Food and Drug act of 1906 do? - 🧠ANSWER
✔✔prohibited interstate sale of adulterated and misbranded food and drugs
and addresses some product labeling issues
what were the product labeling issues addressed in the pure food and drug
act? - 🧠ANSWER ✔✔-labels cannot be false or misleading about
ingredients
-no requirement to disclose ingredients
-11 dangerous ingredients were identified but could be used as long as
listed (cocaine, heroine, ect)
what did the pure food and drug act of 1906 lead to? - 🧠ANSWER ✔✔the
creation of the modern day food and drug administration (FDA)
COPYRIGHT©PROFFKERRYMARTIN 2025/2026. YEAR PUBLISHED 2025. COMPANY REGISTRATION NUMBER: 619652435. TERMS OF USE.
1
PRIVACY STATEMENT. ALL RIGHTS RESERVED
,what is the Sulfanilamide tragedy of 1937? - 🧠ANSWER ✔✔-Tennessee
drug company marketed "Elixir Sulfanilamide" as a wonder drug for
ailments from gonorrhea to sore throats
-dug contained chemical analog of antifreeze "diethyl glycol"
-killed over 105 people (adults and children) which created a public outcry
-failure to list ingredients or test the safety of those ingredients was not a
violation of the 1906 pure food and drug act
What did the sulfanilamide tragedy lead to? - 🧠ANSWER ✔✔giving
enforcement authority to the federal food, drug, and cosmetic act of 1938
what was the Federal food, drug, and cosmetic act of 1938? - 🧠ANSWER
✔✔set of laws passed by congress in 1938 which gave authority to the US
food and drug administration to oversee the safety of food, drugs, and
cosmetics
what were the FD&C requirements that came from the federal food, drug,
and cosmetic act of 1938? - 🧠ANSWER ✔✔-drug labels must include
directions for safe use
-required pre-market approval for new drugs to ensure safety
-prohibited false therapeutic claims for drugs
COPYRIGHT©PROFFKERRYMARTIN 2025/2026. YEAR PUBLISHED 2025. COMPANY REGISTRATION NUMBER: 619652435. TERMS OF USE.
2
PRIVACY STATEMENT. ALL RIGHTS RESERVED
, -authorized factory inspections
-FDA given regulatory authority over medical devices and cosmetics for the
first time
adulteration definition? - 🧠ANSWER ✔✔-contains any poisonous or
deleterious substance which may render it injuries to uses when used as
directed
-contains any filthy, putrid, or decomposed substance (ie expired drugs)
-prepared, packaged, or held under unsanitary conditions and became
contaminated or rendered injuries
-has a poisonous or deleterious container
-contains an unapproved food or color additive
misbranded definition? - 🧠ANSWER ✔✔-incorrect drug, patient name,
prescriber name, or directions
-is missing poison prevention ot tamper-resistant packaging
-OTC products without "adequate directions for use"
-prescription package/products without "adequate directions for use"
COPYRIGHT©PROFFKERRYMARTIN 2025/2026. YEAR PUBLISHED 2025. COMPANY REGISTRATION NUMBER: 619652435. TERMS OF USE.
3
PRIVACY STATEMENT. ALL RIGHTS RESERVED
