Class II · Moderate risk
Fexofenadine HCL
Labeling: Label Mixup; FEXOFENADINE HCL Tablet, 180 mg may be potentially mislabeled as MULTIVITAMIN/MULTIMINERAL, Tablet, NDC 00536406001, Pedigree: AD62992_8, EXP: 5/23/2014.
National Drug Code
Is NDC 41167-4120-03 recalled?
Allegra Allergy · 1 BOTTLE, PLASTIC in 1 CARTON (41167-4120-3) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Yes — this exact package was recalled
1 FDA recall names the code 41167-4120-03 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 hydrochloride
- Strength
- FEXOFENADINE HYDROCHLORIDE 180 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Chattem, Inc.
- Type
- Human OTC Drug
- Product code
- 41167-4120
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
- 41167-0300 See recall 1
- 41167-0310 See recall 1
- 41167-0320 See recall 1
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