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Each vial of NOVAREL is accompanied by a vial of sterile diluent containing 10 mL of Bacteriostatic Water for Injection, USP containing 0.9% benzyl alcohol

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Note that the FDA does not consider USP monographs in the Dietary Supplement section of USP to be applicable monographs , so any of these substances that are desired for compounding should go through the FDA review process described in Category 1 below

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