Class III · Low risk
Taclonex (calcipotriene and betamethasone dipropionate)
Labeling: Incorrect or missing package insert: the affected product was packaged with an out-of-date package insert (PI) dated February 2014.
National Drug Code
Is NDC 50222-0501-06 recalled?
Taclonex · 40 CARTON in 1 CASE (50222-501-06) / 1 BOTTLE in 1 CARTON / 60 g in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 50222-0501-06 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
- calcipotriene and betamethasone dipropionate
- Strength
- CALCIPOTRIENE HYDRATE 50 ug/g; BETAMETHASONE DIPROPIONATE…
- Form
- Suspension · Topical
- Labeler
- LEO Pharma Inc.
- Type
- Human Prescription Drug
- Product code
- 50222-0501
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
- 50222-0350 Adbry 1
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