Class II · Moderate risk
Carbo-O-Philic 40 Gel 40%
Marketed without an Approved NDA/ANDA: FDA has determined that the products are unapproved new drugs and misbranded.
National Drug Code
Is NDC 54162-0016-15 recalled?
Carbo-O-Philic 40 Gel 40%
Yes — this exact package was recalled
1 FDA recall names the code 54162-0016-15 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.
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 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
- 54162-0007 See recall 2
- 54162-0640 See recall 2
- 54162-0015 See recall 1
- 54162-0335 See recall 1
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