FDAMarch 7, 2017drug
Indian God Lotion Spray Bottle, labeling is in foreign language
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Marked Without An Approved NDA/ANDA: FDA analysis found this product to contain diethyl phthalate, an inactive ingredient in several modified release solid oral dosage forms, making this product unapproved drug for which safety and efficacy have not been establish and therefore, subject to recall.
What to do
FDA enforcement status: Terminated
Brands named
a h focal
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDAHU HU SHENG WEI capsules, 3000 mg, 2-count bottle, labeling is in foreign language2017-03-07
- FDABlack Ant capsules, 4600mg, 4-count blister pack, labeling is in foreign language2017-03-07
- FDAMiraculous Evil Root capsules, 1200 mg, 6-count bottle, labeling is in foreign language2017-03-07
- FDAGERMANY NIUBIAN tablets, 3000mg, 10-count bottle, labeling is in foreign language2017-03-07
- FDAMAX MAN capsules, 3000 mg, 6-count bottle, labeling is in foreign language2017-03-07
- FDAYANSHIJIAONANG capsules, 2000mg, 8-count bottle, labeling is in foreign language2017-03-07
- FDALANG YI HAO CHAONONGSUOPIAN tablets, 500 mg, 8-count bottle, labeling is in foreign language2017-03-07
- FDAYe Lang Shen capsules, 5000 mg, 8-count bottle, labeling is in foreign language2017-03-07
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