Ingredients Sample Clauses

Ingredients. All ingredients namely, cement, sand, coarse aggregate and water shall comply with the specifications already listed.
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Ingredients. The diluent is an AMP, bicine, barbital, aspartate buffer with sodium azide added as a preservative. WARNING: FOR IN-VITRO DIAGNOSTIC USE ONLY. DO NOT INGEST. Refer to Sodium Azide Warning.
Ingredients. In the AAA-provider agreement, the AAA shall indicate the method by which the provider shall offer ingredient information on the meals provided to consumers.
Ingredients. (1) The Producer must grow, raise, or catch the ‘defining ingredient’ (e.g., clams in clam chowder, tomato in tomato sauce, basil in pesto, beef in beef stew).
Ingredients. For raw materials, master batches, fillers, inserts and packaging are the prices generally established on an annual basis. Yearly we can negotiate for standard ingredients with the help of our provisions for annual contracts. For custom made products, such as inserts we need to keep our project price due to be in line with our customer project price. Quadrant CMS wish to receive the best prices on first quotations.
Ingredients. Xxxxxx agrees to use the New Ingredient Declaration whenever an ingredient declaration is used. Exhibit E1 (Expanded Lash Warning Statement) Warning: For external use. Avoid getting in eyes; if so, immediately rinse thoroughly with cool water. Not for use by customers under the age of 18. Do not use on damaged or irritated skin, if pregnant or nursing or undergoing treatment for glaucoma or cancer. Not recommended if you have ever experienced dry eyes, eye infections, styes or any other eye-related disorder. If redness, irritation or other unwanted effects occur, stop using product immediately. If symptoms persist, seek medical attention. Keep out of reach of children. (Expanded Brow Warning Statement) Warning: For external use. Avoid getting in eyes; if so, immediately rinse thoroughly with cool water. Not for use by customers under the age of 18. Do not use on damaged or irritated skin, if pregnant or nursing, undergoing treatment for glaucoma or cancer or if you are being treated for a facial skin condition. If redness, irritation or other unwanted effects occur, stop using product immediately. If symptoms persist, seek medical attention. Keep out of reach of children. (Expanded Hair Warning Statement) Warning: For external use. Avoid getting in eyes; if so, immediately rinse thoroughly with cool water. Not for use by customers under the age of 18. Do not use on damaged or irritated skin, if pregnant or nursing, undergoing treatment for glaucoma or cancer, or if you are being treated for a scalp condition. If redness, irritation or other unwanted effects occur, stop using product immediately. If symptoms persist, seek medical attention. Keep out of reach of children. Exhibit E2 (Expanded Lash Instructions for Use) Directions: As with all cosmetic products used in the area of the eye (or close proximity to the eye), it is important to carefully read all directions and warnings. Carefully apply GrandeLASH- MD once daily on a clean, dry upper lash line only using a single stroke on your eyelid just above your upper lash line (like a liquid eyeliner). Do not apply to the lower lash line. Apply only with the product applicator provided. Use one dip into the bottle for both upper lash lines and allow 2-3 minutes for the serum to fully dry before lying down or applying other products to your eye area. Use sparingly. If serum gets into the eye, immediately rinse thoroughly with cool water to completely remove serum from the eye. Apply every day for a full 3 mon...
Ingredients. The buffer is a tris-barbital-sodium barbital buffer. WARNING: FOR IN-VITRO DIAGNOSTIC USE. DO NOT INGEST. The buffer contains barbital which, in sufficient quantity, can be toxic. Preparation for Use: Dissolve one package in 750 mL deionized water. The buffer is ready for use when all material is completely dissolved. Storage and Stability: The packaged buffer should be stored at 15 to 30°C and is stable until the expiration date indicated on the package. Diluted buffer is stable for two months at 15 to 30°C. Signs of Deterioration: Discard packaged buffer if the material shows signs of dampness or discoloration. Discard diluted buffer if it becomes turbid.
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Ingredients. The powder contains anionic and nonionic surfactants, sodium carbonate, enzymes and sodium chloride WARNING: FOR IN-VITRO DIAGNOSTIC USE. Preparation for Use: Dissolve the powder in 8 L of deionized water and mix thoroughly. Storage and Stability: Store the dry powder at 15 to 30°C until the expiration date indicated on the label. The dissolved solution is stable for 1 month when stored at 15 to 30°C. Signs of Deterioration: The dissolved solution should be discarded if it shows signs of bacterial contamination.
Ingredients. No ingredient, including, but not limited to, a flavor used in the recipes of the Business is owned or procurable exclusively through Seller and/or its affiliates.
Ingredients. The calibrator consists of a lyophilized citrated normal human plasma assayed for fibrinogen using a functional clotting assay.2 Refer to the enclosed package insert for the assay value. CAUTION: FOR IN-VITRO DIAGNOSTIC USE The Helena Fibrinogen Calibrator has been found negative for Hepatitis B Antigen (HBsAg) and HIV antibody; however, this plasma should be handled with the same precaution as any human plasma sample. Avoid ingestion.
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