Vol. 31, No. 5, September–October 2012, pp. 717–737
ISSN 0732-2399 (print) ISSN 1526-548X (online)
http://dx.doi.org/10.1287/mksc.1110.0692
© 2012 INFORMS
Unintended Nutrition Consequences:
Firm Responses to the Nutrition Labeling and
Education Act
Christine Moorman
Fuqua School of Business, Duke University, Durham, North Carolina 27708, moorman@duke.edu
Rosellina Ferraro
Robert H. Smith School of Business, University of Maryland, College Park, Maryland 20742,
rferraro@rhsmith.umd.edu
Joel Huber
Fuqua School of Business, Duke University, Durham, North Carolina 27708, joel.huber@duke.edu
T
his paper investigates how firms responded to standardized nutrition labels on food products required by
the Nutrition Labeling and Education Act (NLEA). Using a longitudinal quasi-experimental design, we test
our predictions using two large-scale samples that span 30 product categories. Results indicate that the NLEA
reduced brand nutritional quality relative to a control group of products not regulated by the NLEA. At the
same time, among regulated products, brand taste increased. Although this reduction in nutrition represents an
unintended consequence of regulation, there were a set of category, firm, and brand conditions under which the
NLEA produced a positive effect on brand nutritional quality. We find that firms were more likely to improve
brand nutrition when firm risk or firm power is low. Lower risk occurs when the firm is introducing a new
brand rather than changing an existing brand, and weaker power in a category is reflected by lower market
share in a category. Furthermore, firms competing in low-health categories (e.g., potato chips) or small-portion
categories (e.g., peanut butter) improved nutrition more than firms competing in high-health categories (e.g.,
bread) or large-portion categories (e.g., frozen dinners). Recommendations for firm strategy and the design of
consumer information policy are examined in light of these surprising firm responses.
Key words : nutrition labels; nutrition; taste; firm strategy; public policy; quality information
History : Received: August 14, 2009; accepted: October 26, 2011; Eric Bradlow served as the editor-in-chief and
Scott Neslin served as associate editor for this article. Published online in Articles in Advance February 16,
2012; revised July 12, 2012.
1. Introduction
The Nutrition Labeling and Education Act (NLEA)
sought to eliminate untruthful nutrition claims and
to improve consumers’ abilities to access and process
nutrition information at the point of sale. It required
manufacturers to provide a “Nutrition Facts” label
displaying standardized information on all nutrients,
recommended daily values, and an ingredient list on
food products by May 1994 (Federal Register 1993).
Health claims making diet–disease links or using
terms such as “light” were also regulated for truthful
content.
Before the act, nutrition labels were required only
when manufacturers made an explicit nutrition claim
in advertising or on the package (e.g., low sodium) or
when the product was fortified with additional nutri-
ents (Federal Register 1973).
1
As a result, prior to the
1
The required nutrition information was serving size, number of
servings per container, calories, carbohydrates, protein, and fat per
NLEA, most food products did not disclose nutrition
information, making comparisons within and across
categories difficult for consumers. Furthermore, even
those products providing nutrition information did
not list recommended daily values for important
nutrients such as fat, sodium, and cholesterol.
Theory suggests that the NLEA’s required labels
should promote consumer search and, in turn, stim-
ulate competition to improve brand nutrition lev-
els (e.g., Salop 1976, Stigler 1961). As noted by the
Federal Trade Commission (1979, p. 14), “Informa-
tion remedies have the direct benefit of improving
the free flow of truthful commercial information.
Informed consumer decisions then give sellers an eco-
nomic incentive to improve the quality and selec-
tion of their marketplace offerings.” This logic may
serving, as well as percent Recommended Daily Allowances for
protein, vitamins A and C, thiamine, riboflavin, niacin, calcium,
and iron. In 1985, the rule was expanded to include sodium per
serving.
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