Class II · Moderate risk
Severe Congestion Nasal Spray
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
National Drug Code
Is NDC 41520-0108-10 recalled?
CareOne Severe Congestion Nasal · 1 BOTTLE, SPRAY in 1 CARTON (41520-108-10) / 30 mL in 1 BOTTLE, SPRAY
Yes — this exact package was recalled
2 FDA recalls name the code 41520-0108-10 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
- American Sales Company
- Type
- Human OTC Drug
- Product code
- 41520-0108
Recalls naming this package
Class II · Moderate risk
Severe Congestion 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
- 41520-0392 See recall 2
- 41520-0431 careone nighttime sleep aid 2
- 41520-0229 CareOne Allergy Relief 1
- 41520-0419 See recall 1
- 41520-0458 See recall 1
- 41520-0525 See recall 1
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