Sentences with phrase «product labeling rules»
In fact, the frequency of cat pyrethrin / pyrethroid toxicity cases resulting from inadvertent (or intentional) application of a dog product to cats was so high that in 2010 the EPA improved product labeling rules for spot - on products for pets to help prevent these inadvertent and intentional species «mix - ups.»
https://www.preventivevet.com/ Not exact matches
A new rule makes it tough for anyone but the government to sue companies for labeling products with outdated patent numbers (which happened to Frisbee and Wooly Willy).
The Food and Drug Administration recently passed new labeling rules for gluten - free products.
FritoLay's official statement for this chip on their page for gluten - free and products without gluten ingredients is the product «contain less than 20 ppm of gluten, the level put forward in the FDA's Gluten Free Food Labeling Final Rule».
The EU legislation governing organic farming, namely «Council Regulation No 834 / 2007 / EC of 28 June 2007 on organic production and labelling of organic products and repealing Regulation No 2092 / 91 / EEC and its detailed implementing rules (Commission Regulation (EC) No 889/2008)», lays down the precise production and manufacturing requirements for agricultural produce and foods labelled as organic products.
The code establishes rules for own - label products and for suppliers» intellectual property and «innovation» rights.
Wine Industry Divided over Proposed Bottle Labeling Rule Though wineries throughout the U.S. regularly source wine grapes grown in Napa Valley, the right for winemakers to call their finished product «Napa Valley» wine may soon extend only to the California state line...
The rule for the label's use on poultry products, for example, is merely that outdoor access be available for «an undetermined period each day.»
The Malaysian Guide to Nutrition Labelling and Claims (as at December 2010) establishes rules on the use of nutrient content claims (ie levels of fat for a low - fat claim) and nutrient comparative claims (eg comparison between an old and new product formulation).
At TTB, Busey was regarded for his depth of knowledge in product formulation and labeling, as well as importation and exportation requirements and documentation rules, including regulatory history and institutional knowledge regarding agency enforcement policies.
The USDA has ruled that the product is beef and should be labeled as such.
The European Parliament today voted today — 393 votes in favour, 305 votes against — to reject draft EU rules on baby food, which would have allowed baby foods to contain high levels of sugar and products to be labelled for use from 4 months of age.
Members of the European Parliament (MEPs) voted on 19 January 2016 (393 votes in favour, 305 votes against) to reject draft EU rules on baby food, which would have allowed baby foods to contain high levels of sugar and products to be labelled for use from 4 months of age.
To the extent that the information required to be marked on the product (by the tracking label requirement and the registration card rule) is duplicative, you may combine the markings on the product to satisfy both requirements.
The rule for the label's use on poultry products, for example, is merely that outdoor access be available for «an undetermined period each day.»
The only problem, industry representatives say, is that current federal rules on such products require prominent «reduced calorie» labeling on the front of the package, which is «not attractive to children» and contributes to an «overall decline in milk consumption.»
A good rule of thumb is to always read labels and steer clear of products that contain the words «hydrogenated» or «partially hydrogenated oils.»
Found to cause cancer in lab rats in the 1970's, consequently the FDA imposed a warning label on saccharin products but after a 3 - decade long effort bt Monsanto to reverse this ruling, in 2001 they won and American consumers lost.
Under current Food and Drug Administration rules, a product can be labeled «gluten - free» if it has 20 parts per million (ppm) of gluten or less.
Certified 100 % Organic means that all the ingredients in a product have been grown or raised according to the USDA's organic standards, which are the rules for producing foods labeled organic.
The Fda even has a rule in location that says if most of the Gluten is removed, then the meals product can be labeled Gluten - Free.
The United States Department of Agriculture (USDA) certifies organic products through their National Organic Program (NOP), which develops rules and regulations for the production, handling, labeling of all USDA organic products.
Raj Nair, Ford's group vice president of global product development, told reporters those rules date «back to the 1970s, and they were created by the EPA as a general means to provide fuel economy labels without having to test every single vehicle in the industry.»
As a general rule, store all cleaning products in a secure cabinet out of the reach of pets and keep them in their original packaging, or in a clearly labeled and tightly sealed container.
It is the state feed control official's responsibility in regulating pet food to ensure that the laws and rules established for the protection of companion animals and their custodians are complied with so that only unadulterated, correctly and uniformly labeled pet food products are distributed in the marketplace and a structure for orderly commerce.
Secondly there is a gap in the standard, known as the «family rule,» this is where a label can state that tests were completed if it's «similar» to a product that was tested on animals.
The CJEU ruling would significantly curtail a generic player's ability to file applications with excised or skinny labels in situations where the first indication even after enjoying its ten year exclusivity period is nonetheless protected by the orphan exclusivity of a second similar product and the remaining indications are protected by patents.
Our attorneys have considerable experience in all of the legal issues affecting a business's ability to promote its offerings, including claim substantiation, Lanham Act false advertising, social media promotions, state unfair competition, First Amendment protection for commercial speech, FDA labeling rules, trademark, copyright, product disparagement, right of publicity, keyword advertising disputes, sweepstakes and contests, privacy and data security.
Thus, in the final rule, we allow covered entities to disclose protected health information to entities subject to FDA jurisdiction for the following activities: To report adverse events (or similar reports with Start Printed Page 82670respect to food or dietary supplements), product defects or problems (including problems with the use or labeling of a product), or biological product deviations, if the disclosure is made to the person required or directed to report such information to the FDA; to track products if the disclosure is made to a person required or directed by the FDA to track the product; to enable product recalls, repairs, or replacement (including locating and notifying individuals who have received products of product recalls, withdrawals, or other problems); or to conduct post-marketing surveillance to comply with requirements or at the direction of the FDA.