One and Zen recalls GINSENG KIANPI PIL, 60 capsules, PRODUCT OF KWEILIN DRUG MANUFACTORY
Recalled January 7, 2015 · FDA recall D-0329-2015 · One and Zen
Hazard
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. · FDA Class II
Units
38 bottles
Sold at
Nationwide
Description
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
GINSENG KIANPI PIL, 60 capsules, PRODUCT OF KWEILIN DRUG MANUFACTORY
Manufacturer(s)
One and Zen
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →