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Are you ready for new alcoholic beverage labeling and advertising regs that make room for wine in a box and the need to comply with FDA regulations? (New TTB advertising and labeling rules Part 3)

new regulations for advertising and labeling malt beverages (craft beer), wine, and distilled spirits

The TTB looks to update the rules and regulations regarding the labeling and advertising of wine, malt beverages (craft beer), and distilled spirits

The next few installments of our ongoing series reviewing the new proposed rules in the TTB’s Notice 176 – the Modernization of the Labeling and Advertising Regulations for Wine, Distilled Spirits, and Malt Beverages – will highlight the specific proposed changes to the Subparts of 27 CFR 4, 5, and 7.

Proposed changes to Subpart A (General Provisions) for Parts 4, 5, and 7 of 27 CFR:

Definitions will be added to the terms brand name, certificate holder, certificate of exemption from label approval, certificate of label approval (COLA), distinctive or fanciful name, and net contents.  These definitions will track the common understanding and procedures currently used by the TTB:

The term advertisement is also removed from the definitions as it is now part of its own proposed part, 27 CFR part 14.

Also of note, the proposal notes in the General Provisions amendments that 27 CFR sections 4.9, 5.9 and 7.9 will be updated to provide that it is the responsibility of the industry member to ensure that any ingredient used in production of alcoholic beverages complies with the applicable Food and Drug Administration (FDA) regulations pertaining to the safety of food ingredients and additives and that the TTB may at any time request documentation to establish such compliance. In addition the sections provide that it remains the responsibility of the industry member to ensure that their containers are made of suitable materials to comply with all applicable FDA health and safety regulations for the packaging of alcoholic beverages for consumption and that the TTB may at any time request documentation to establish such compliance.

Also the notes to the General Provisions note that is the TTB’s long-standing position that review and approval of labels and formulas doesn’t relieve the industry member from its responsibility to ensure compliance with applicable FDA regulations. The new regulations will also contain at sections 4.10, 5.10, and 7.10, a list of regulations implemented by other federal agencies of which industry members should be aware.

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