SUPER HERBS 350 mg, 30 capsules per bottle.

Recall Number: D-0909-2016

Firm: Super Herbs

Classification: Class I

Status: Terminated

Report Date: 20160601

Initiation Date: 20151123

Termination Date: 20241001

Reason for Recall

Marketed without an approved NDA/ANDA - presence of undeclared sibutramine, desmethylsibutramine (an active metabolite of sibutramine) and/or phenolphthalein.

Product Description

SUPER HERBS 350 mg, 30 capsules per bottle.

DrugLabelsHub provides FDA drug labeling information for reference only. Always consult a healthcare professional.

Data source: openFDA · Updated regularly