Class II · Moderate risk
CAREONE Allergy Relief
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
National Drug Code
Is NDC 41520-0229-39 recalled?
CareOne Allergy Relief · 1 BOTTLE in 1 CARTON (41520-229-39) / 30 TABLET, FILM COATED in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 41520-0229-39 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
- fexofenadine hcl
- Strength
- FEXOFENADINE HYDROCHLORIDE 180 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- American Sales Company
- Type
- Human OTC Drug
- Product code
- 41520-0229
Recalls naming this package
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
- 41520-0108 CareOne Severe Congestion Nasal 2
- 41520-0392 See recall 2
- 41520-0431 careone nighttime sleep aid 2
- 41520-0419 See recall 1
- 41520-0458 See recall 1
- 41520-0525 See recall 1
Free recall alerts
Know the day your medication is recalled
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