Class II · Moderate risk
Maximum Strength Nasal Spray
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
National Drug Code
Is NDC 41250-0989-10 recalled?
nasal · 1 BOTTLE in 1 CARTON (41250-989-10) / 30 mL in 1 BOTTLE
Yes — this exact package was recalled
2 FDA recalls name the code 41250-0989-10 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
- oxymetazoline hydrochloride
- Strength
- OXYMETAZOLINE HYDROCHLORIDE .05 g/100mL
- Form
- Spray · Nasal
- Labeler
- Meijer Distribution Inc
- Type
- Human OTC Drug
- Product code
- 41250-0989
Recalls naming this package
Class II · Moderate risk
Maximum Strength Nasal Spray
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
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
- 41250-0852 See recall 3
- 41250-0708 See recall 2
- 41250-0718 Meijer Dry Eye Relief 2
- 41250-0060 See recall 1
- 41250-0106 See recall 1
- 41250-0252 See recall 1
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