Class III · Low risk
Ciclopirox Olamine Cream USP
Discoloration: Product is supposed to be a white to off white homogenous cream and may have intermittent yellow discoloration.
National Drug Code
Is NDC 0713-0638-15 recalled?
Ciclopirox Olamine · 1 TUBE in 1 BOX (0713-0638-15) / 15 g in 1 TUBE
Yes — this exact package was recalled
2 FDA recalls name the code 0713-0638-15 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
- Ciclopirox Olamine
- Strength
- CICLOPIROX OLAMINE 7.7 mg/g
- Form
- Cream · Topical
- Labeler
- Cosette Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 0713-0638
Recalls naming this package
Class III · Low risk
Ciclopirox Olamine Cream USP
Labeling: Incorrect or Missing Package Insert: product lots packaged with an out-of-date insert.
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
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.