Class II · Moderate risk
Pure Care Foaming Mint Hand Sanitizer 62%
CGMP Deviations
National Drug Code
Is NDC 75009-0562 recalled?
Pure Care Foaming Mint Hand Sanitizer 62%
This product was recalled — in other package sizes
No FDA recall names your exact package code, but 1 recall cover the same product (75009-0562) in a different bottle or carton size. Worth checking with your pharmacist.
This code is not in the current FDA NDC directory — usual for a product that has since been discontinued or repackaged. The details below come from the recall notices themselves.
Recalls of this product
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.
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.