GINSENG KIANPI PIL, 60 capsules, PRODUCT OF KWEILIN DRUG MANUFACTORY
Recall Number: D-0329-2015
Firm: One and Zen
Classification: Class II
Status: Terminated
Report Date: 20150107
Initiation Date: 20141120
Termination Date: 20150323
Reason for Recall
Marketed Without An Approved NDA/ANDA: FDA analysis found this product to contain undeclared dexamethasone and cyproheptadine which are FDA approved drugs making this product an unapproved drug.
Product Description
GINSENG KIANPI PIL, 60 capsules, PRODUCT OF KWEILIN DRUG MANUFACTORY