Aerospan tm (flunisolide hfa, 80 mcg) Inhalation Aerosol For Oral Inhalation Only Rx Only description

 
HOW SUPPLIED 
AEROSPAN Inhalation Aerosol is supplied as a pressurized lined aluminum canister in 
boxes of one. Each canister is supplied with a two-piece plastic purple actuator and gray 
spacer assembly, and tear-off patient’s instructions, including a Patient Information and 
an illustrated Instructions for Using Your AEROSPAN Inhalation Aerosol.
The following canister sizes are available: 8.9 g net weight, providing 120 metered 
actuations (trade size, NDC 0456-5550-12); 5.1 g net weight providing 60 metered 
actuations (hospital size, NDC 0456-5550-63); 5.1 g net weight providing 60 metered 
actuations (professional sample, NDC 0456-5550-06). 
When not in use, keep AEROSPAN Inhalation Aerosol out of reach of children.
Pediatric patients should only administer AEROSPAN Inhalation Aerosol under adult 
supervision.
The plastic purple actuator and gray spacer assembly supplied as part of AEROSPAN 
Inhalation Aerosol should not be used with any other product canisters; and the actuator 
from other products should not be used with an AEROSPAN Inhalation Aerosol canister.
Do not separate the purple actuator from the gray spacer. Do not use this product with 
any external spacer devices.
The labeled amount of medication in each actuation cannot be assured after 120 metered 
actuations (or 60 metered actuations in the hospital and sample size canisters), even 
though the canister is not completely empty and will continue to operate. The inhaler 
(canister plus actuator) should be discarded when the labeled number of actuations have 
been used. Never immerse the canister into water to determine the amount of 
formulation remaining in the canister (“float test”). 
Store at 25 °C (77 °F); excursions permitted to 15 – 30 
°
C (59 – 86 
°
F) [see USP 
Controlled Room Temperature].
For best results, the canister should be at room 
temperature before use.