Bee Xtreme: Marketed without an Approved NDA/ANDA; FDA analysis found them to contain sibutramine and phenolphthalein

Agency Publication Date: October 12, 2016

Affected Products

Product: La' Trim Plus Dietary Supplement Capsules, 350 mg, 60 count bottles, Manufactured for Timeless Solutions, 1810 E Sahara Ave #100, Las Vegas, Nevada 89104, distributed by BeeXtreme LLC, Punxsutawney PA

All Lots

Product: Oasis Dietary Supplement Capsules, 500 mg, 45 count bottles, Manufactured for Timeless Solutions, 1810 E Sahara Ave #100, Las Vegas, Nevada 89104, distributed by BeeXtreme LLC, Punxsutawney PA

All Lots

Product: Jenesis Dietary Supplement Capsules, 350 mg, 60 count bottles, Manufactured for Timeless Solutions, 1810 E Sahara Ave #100, Las Vegas, Nevada 89104, distributed by BeeXtreme LLC, Punxsutawney PA

All Lots

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 73167

Status: Resolved

Manufacturer: Bee Xtreme

Manufactured In: United States

Units Affected: 3 products (589 bottles; 732 bottles; 13 bottles)

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Sources: FDA iRES · Raw API Response

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Affected Products

All Lots