PRACTICE WITH PRECISION
Pr NUCEIVA TM is designed with precision to put control in the hands of the provider.
WHAT’S IN THE VIAL
900 kDa
100U vial
2.5mL diluent
MOLECULAR MASS
VIAL
RECONSTITUTION
A botulinumtoxin type A that is purified from clostridium botlulinum.
Reconstitute the 100 unit vial with 2.5mL preservative-free 0.9% sodium chloride injection (not included) to obtain a concentration of 4 Units/0.1mL
100 units of botulinum toxin type A neurotoxin complex, 0.5 mg human serum albumin (HSA), and 0.9 mg sodium chloride (NaCl). Sterile, vacuum-dried without a preservative and stored at 2-8 º C
INDICATIONS AND USAGE Pr NUCEIVA TM is indicated for the temporary improvement in the appearance of moderate to severe glabellar lines in adult patients < 65 years of age. SERIOUS WARNINGS AND PRECAUTIONS DISTANT SPREAD OF TOXIN EFFECT: The e ects of NUCEIVA and all botulinum toxin products may spread from the area of injection to produce symptoms consistent with botulinum toxin e ects. These symptoms have been reported hours to weeks a er injection. Swallowing and breathing di culties can be life-threatening and there have been reports of death. The risk of symptoms is probably greatest in children treated for spasticity, but symptoms can occur in adults, particularly in those patients who have underlying conditions that would predispose them to these symptoms.
6
Made with FlippingBook interactive PDF creator