Harris Teeter raises more than $340,000 for JDRF
CHARLOTTE, N.C. — Harris Teeter on Monday donated more than $340,000 to JDRF, made possible thanks to contributions from Harris Teeter customers during the company’s recent point-of-purchase campaign.
Harris Teeter hosted the point of purchase donation card campaign in March, during which time Harris Teeter customers were invited to make $1, $3 or $5 donations to JDRF at checkout.
“Harris Teeter customers continue to show their generosity to our nonprofit partners,” stated Catherine Becker, communication manager for Harris Teeter, “and we appreciate their overwhelming support of JDRF.”
In addition to the donation from the point of purchase donation card campaign, Harris Teeter also is sponsoring the upcoming Harris Teeter Celebrity Golf Classic benefiting the Greater Western Carolinas Chapter of JDRF on May 8, 2013 here. For more than 10 years, Harris Teeter has been a sponsor of the golf classic and in that time, the Greater Western Carolinas Chapter of JDRF has generated more than $900,000 for T1D research from the golf tournament.
Grocer Weis Markets posts first-quarter sales increase of 3.2%
SUNBURY, Pa. — Weis Markets on Monday posted first-quarter sales of $682.7 million, representing an increase of 3.2%. Same-store sales were up 0.8%.
"We continue to make forward progress in a market impacted by a poor economy that is generating minimal job growth. These have been ongoing trends in most of the markets we serve," said David Hepfinger, Weis Markets’ president and CEO. "Our customers also were impacted in the first quarter by a tax increase and post-holiday debt," he said.
The soft sales environment fosters heightened competitive activity, Hepfinger added. "We were able to offset these trends through disciplined marketing and promotional programs and improved productivity and operational efficiencies at store and distributional levels."
Industry urges FDA to clarify new dietary ingredient notification regulations
SILVER SPRING, Md. — The five associations representing the dietary supplement industry on Monday requested that the Food and Drug Administration issue revised guidance on new dietary ingredient notifications, with a specific focus on the information to be included to identify the new dietary ingredient.
The request, made by the American Herbal Products Association, the Council for Responsible Nutrition, the Consumer Healthcare Products Association, the Natural Products Association and the United Natural Products Alliance, was made in the form of comments submitted by AHPA to FDA on April 27 and joined by CRN, CHPA, NPA and UNPA in separate submissions.
The groups note that FDA’s rule on NDI notifications does not specifically state what information should be provided to the agency on the identity of the ingredient that is the subject of an NDI notification. Yet the most common objection communicated by FDA in its responses to NDI notifications is that the agency “is unable to establish the identity” of the dietary ingredient that is the subject of the notification.
“This is clearly an area in which guidance is needed by the regulated supplement industry,” stated Michael McGuffin, AHPA president. “We are therefore requesting that the FDA prioritize its attention to this specific issue and provide the industry with clarity on this matter.”
Earlier comments submitted by each of the trade associations to the FDA’s June 2011 draft guidance, "Dietary Supplements: New Dietary Ingredient Notifications and Related Issues," generally were critical. In June 2012, the FDA informed the associations that the agency was planning to promulgate revised draft NDI guidance and would permit additional input from the industry on these topics.
“Other issues raised by the FDA’s 2011 draft NDI guidance are still concerning to the supplement industry,” noted Steve Mister, president and CEO of CRN. “We will continue our active dialogue with the FDA until each of these is resolved. But in the meantime, it benefits both the industry and FDA to move forward on the topics where there is agreement. What constitutes an adequate description of the ingredient in an NDI notification is one of those issues where the trade associations and the FDA are likely to agree.”
One of the bigger issues includes which supplements have been grandfathered under the regulation, and subsequently don’t need an NDI, and which haven’t. “We must continue our discussions about what demonstrates whether an ingredient is grandfathered under the law, what constitutes chemical alteration of an old ingredient, and other matters," acknowledged Scott Melville, CHPA president and CEO. "However, there’s no need to hold up guidance on this issue while we continue discussions on the meaning of the statute in other areas.”