Label Requirements Sample Clauses
The Label Requirements clause sets out the standards and obligations for labeling products or materials covered by the agreement. It typically details what information must appear on labels, such as product names, safety warnings, regulatory compliance marks, or batch numbers, and may specify the format, language, and placement of such labels. This clause ensures that all products are properly identified and meet legal or contractual labeling standards, thereby reducing the risk of regulatory violations, misidentification, or consumer confusion.
POPULAR SAMPLE Copied 1 times
Label Requirements. The label must include in the “DIRECTIONS FOR USE” section the following statements:
1) “This product may not be reformulated or repackaged into another product unless the registration of the reformulated or repackaged product was either granted or amended after May 1, 2004 so as to be consistent with the terms and conditions set forth in the Atrazine January 31, 2003 Interim Reregistration Eligibility Document (IRED).” The terms and conditions of the IRED will be consistent with the Agreement.
2) “No product (other than products containing 4% or less atrazine active ingredient) may be formulated or repackaged from this product unless the formulated repackaged product bears a label including all of the following statements: The following language must be prominently displayed in the DIRECTIONS FOR USE on the label: “ANY USE OF THIS PRODUCT IN AN AREA WHERE USE IS PROHIBITED IS A VIOLATION OF FEDERAL LAW. Before using this product, you must consult the Atrazine Watershed Information Center (AWIC) to determine whether the use of this product is prohibited in your watershed. AWIC can be accessed through ▇▇▇.▇▇▇▇▇▇▇▇-▇▇▇▇▇▇▇▇▇.▇▇▇▇ or ▇-▇▇▇-▇▇▇-▇▇▇▇ [or insert own AWIC contact information]. If use of this product is prohibited in your watershed, you may return this product to your point of purchase or contact [insert name of registrant] for a refund.””
3) No products containing 4% or less active ingredient may be formulated or repackaged from this product unless the registration of the resulting product includes the following terms and conditions: the Registrant of this product shall immediately: i) cease all distribution and sale to any retailer or any entity distributing or selling such product to any retailer located within all counties containing any portion of any Watershed Area listed in the AWIC; ii) ensure the removal of such Atrazine product from the shelves of any retailer located within all counties containing any portion of any Watershed Area listed in the AWIC; and iii) repurchase any such Atrazine product from any of the purchasers described above. In addition, such Registrant shall consult with the State(s) in which such counties are located to determine whether additional territory shall be included in the area to which these requirements will apply. If the State(s) determine that a larger area is warranted, the Registrant shall within 10 days of such determination notify the Director of EPA’s Special Review and Reregistration Division (SRRD) (...
Label Requirements. An intentional radiator device subject to certification by the FCC shall carry a warning label which includes the following statement:
Label Requirements. Subject to the terms of Section 2.6 ("Trademark License for Immersion") and Section 2.7 ("Administration Procedure"), Logitech shall place belly labels on Gaming Devices which are Royalty Bearing Products which shall include the language and related logo: "I-Force(TM) Force Feedback Technology Licensed from Immersion Corporation" (hereinafter the "Legend"). Logitech shall also place or have placed the Legend on retail manuals and boxes as designated in Exhibit B ("Immersion Package Labeling Specification"). If OEM customers object to belly label marking, the Parties will mutually agree upon a reasonable solution in writing in advance. Logitech shall not remove Immersion's copyright notices from any copies of the Immersion Software.
Label Requirements. Subject to the terms of Section 2.6 ("Trademark License for Immersion") and Section 2.7 ("Administration Procedure"), Logitech shall place belly labels on Force Feedback Cursor Control Devices which are Royalty Bearing Products which shall include the language and related logo: "FEELitTM Force Feedback Technology Licensed from Immersion Corporation" (hereinafter the "Legend"). Logitech shall also place or have placed the Legend on retail manuals and boxes as designated in Exhibit B ("Immersion Package Labeling Specification"). Logitech shall not remove Immersion's copyright notices from any copies of the Immersion Software. The parties agree that in the case of each Planar Force Feedback Cursor Control Device noticed by Logitech to Immersion under the terms of Section 2.7 ("Administrative Procedures"), Immersion will provide Logitech with a list of applicable Licensed Patents which will identify the "Key Licensed Patents" which will be identified on the belly label of the particular device and will also identify the "Document Patents" which will be identified in the product documentation included with the device. The language on the belly label for the Key Licensed Patents will read as follows: "{List Key License Patents} and other patents listed in associated documentation." If OEM customers object to belly label marking or the inclusion of patents in the documentation as described above, the Parties will mutually agree upon a reasonable solution in writing in advance.
Label Requirements. In accordance with Exhibit B, Samsung agrees to use commercially reasonable efforts to provide a reference to Immersion’s patents covering the Licensed Software and Immersion Patents by including the information set forth in Exhibit B on an Internet website or manuals designed to be accessed by end users (located in the United States) of Licensed Devices.
Label Requirements. An intentional radiator device subject to certification by the FCC shall carry a warning label which includes the following statement: (Due to space limitation, this statement will be shown on Users’ Manual Page ii.)
Label Requirements. Product labels must include the following: Once the unit is repaired (a) the CPC prefix would change from “A0” (e.g., AO23456) to “AR” (i.e., the example would change to AR23456), (b) the repair date would be stamped under the manufacture date.
Label Requirements. Qiagen shall package and label Products and Epoch Primers in standard Qiagen packaging. Such packaging shall include, in a manner that is reasonably prominent in position and size: (a) "Powered by innovation from Epoch," and (b) "For Research Use Only."
Label Requirements. All labeling for the Products will contain the Epoch and Amersham names and logos in equal prominence, designating Epoch as the manufacturer and Amersham as the distributor. All advertising and catalogue entries with respect to the Products shall include, in a manner that is reasonably prominent, the name "Epoch MGB Eclipse," or other mutually agreed upon designation, and an acknowledgement that Epoch is the manufacturer of such Product. Amersham may only resell Products that contain a label that clearly and conspicuously states and includes the following: (a) that the Products are for research purposes only, and may not be used for any other commercial, clinical, diagnostic or any other use, and (b) that more information regarding the foregoing can be found in the product insert accompanying such Product.
Label Requirements. SUPPLIER PACKAGE SEAL LABEL