Class II · Moderate risk
Dymista (azelastine hydrochloride and fluticasone propionate)
Defective Container: Potential for broken glass in the neck area of the glass bottles.
National Drug Code
Is NDC 0037-0245-23 recalled?
Dymista · 1 BOTTLE, SPRAY in 1 BOX (0037-0245-23) / 120 SPRAY, METERED in 1 BOTTLE, SPRAY
Yes — this exact package was recalled
2 FDA recalls name the code 0037-0245-23 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Azelastine Hydrochloride and Fluticasone Propionate
- Strength
- AZELASTINE HYDROCHLORIDE 137 ug/1; FLUTICASONE PROPIONATE…
- Form
- Spray, Metered · Nasal
- Labeler
- Viatris Specialty LLC
- Type
- Human Prescription Drug
- Product code
- 0037-0245
Recalls naming this package
Class II · Moderate risk
Dymista (azelastine hydrochloride and fluticasone propionate)
Presence of foreign substance: Potential for glass in the neck area of the glass bottles.
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
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