Whether bottled water is packaged in
small containers sold in a store
or in coolers in the home and office, federal and
state governments regulate it, and the industry also has standards that member
companies must follow to help ensure consumers enjoy a safe, high quality
product.
Federal
While the Environmental Protection Agency (EPA)
regulates tap water as a utility, the Food and Drug Administration (FDA)
regulates bottled water as a packaged food product. FDA bottled water
regulations include:
Standard of Identity—FDA requires uniform use of terms like "purified" and "spring," so
consumers can be sure different companies use the same descriptions consistently
on their product labels. For example, a bottle marked "spring water" must be
from a spring. One-fourth of bottled water comes from municipal sources, rather
than a spring or well. The FDA requires these products be labeled "from a
community water system" or "from a municipal source." However, if this water
goes through a purification process such as distillation or reverse osmosis, FDA
has determined that the product can be defined by the type of purification
(i.e.; "drinking water"), rather than as from a municipal
source.
Current Good Manufacturing Practices
(GMPs)—for both general food and
bottled water-specific categories. General GMPs govern plant and ground
maintenance and facility sanitation. Bottled water-specific GMPs cover plant
construction and design, equipment design and production, process controls
specific to bottled water, and extensive record keeping. They also require safe
and sanitary transportation and storage.
Standard of Quality (SOQ)—Along with Good Manufacturing Practices, SOQs are specific
bottled water product standards that help ensure safety from production and
packaging to consumption. To ensure compliance, companies must test for
pesticides, minerals, and physical properties such as color. By law, FDA bottled
water SOQs must be at least as stringent and protective of public health as
EPA’s standards for public water supplies. To assure the safety of bottled water, the FDA has developed standards that
set a minimal acceptable level of quality. The quality standards
address
substances in the water that may be harmful to health, as well
as substances
that affect the smell, color, and taste of water. The
quality standards also
require public notification whenever the
microbiological, physical, chemical, or
radiological quality of bottled
water falls below standard. Follow the link to see the National Primary Drinking
Water Regulations and the National Secondary Drinking Water
Regulations.
Bottled Water is also subject to FDA food
recall, mislabeling, and adulteration provisions.
State
States also regulate bottled water. They
are responsible for inspecting, sampling, analyzing, and approving water
sources. States certify testing laboratories and perform unannounced and annual
inspections. Some states have unique bottled water regulations, and many base
their regulations on FDA, and in some cases, industry-based
standards. Domestic bottled water producers that sell their products in other states
(interstate commerce) are subject to periodic, unannounced inspections
by FDA.
Upon inspection, the producers must be in compliance with all
aspects of the
Quality Standards and Good Manufacturing Practices for
bottled water, the Fair
Packaging and Labeling Act, and all other
applicable regulations that are
incorporated in the FDA quality
standards. Domestic bottled water producers are
subject to inspection
by state health officials and must comply with all
applicable state
laws and regulations. Some states (e.g. California,
Pennsylvania, and
Florida) have adopted regulations that are stricter than
federal
requirements.
Industry
The bottled water industry has a comprehensive program of self-regulation.
For example, bottled water producers who are members of the International
Bottled Water
Association (IBWA) are inspected annually by an independent
laboratory, the National Sanitation
Foundation (NSF). Through the unannounced
NSF inspection, IBWA
members are evaluated on their compliance with both the
association's
performance requirements and the FDA regulations.
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