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Answer :
Final answer:
The Federal Anti-Tampering Act primarily requires manufacturers to use tamper-resistant packaging for consumer products, especially pharmaceuticals. This act ensures product safety by implementing measures to prevent unauthorized access. Other related regulations address child safety and prescription requirements, but they are distinct from this act.
Explanation:
Key Feature of the Federal Anti-Tampering Act
The Federal Anti-Tampering Act, passed in the 1980s, primarily focuses on ensuring the safety of consumer products, particularly in the pharmaceutical industry. The key feature of this act is that it requires manufacturers to use tamper-resistant packaging.
This packaging includes various measures designed to prevent unauthorized access to the contents of the product, making it more difficult for tampering to occur. For example, many over-the-counter medications now incorporate seals or breakable caps as part of their packaging to alert consumers if a product has been compromised. Such innovations not only safeguard consumers but also bolster their confidence in the safety of the products they purchase.
In contrast, the other options listed, such as requiring child-resistant containers or the necessity of prescriptions for drugs, are governed by different regulations and acts, including the Poison Prevention Packaging Act and the Controlled Substances Act.
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