American Lifestyle.Com: Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the FDA has determined the Vicerex product contains undeclared tadalafil and the Black Ant product contains undeclared sildenafil. Tadalafil and sildenafil are FDA-Approved drugs used to treat male erectile dysfunction (ED), making the Vicerex and the Black Ant products unapproved new drugs.

Agency Publication Date: April 7, 2014

Affected Products

Product: Vicerex A Powerful And Fast Acting Male Sexual Enhancer, 10 capsules per box, Dietary Supplement. UPC 893490820087 (product numbers may possibly vary for same product identification and same product packaging), distributed by Vicerex.com.

All lots, UPC 893490820087

Product: Black Ant, 4600 mg x 4. Product is packaged in a small green box with gold lettering on the front, the back side of the box contains mostly foreign character. Within the box there are four (4) capsules individually wrapped in black and red plastic with white lettering. UPC 4026666142546 (product numbers may possibly vary for same product identification and same product packaging).

All lots, UPC 4026666142546.

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 65095

Status: Resolved

Manufacturer: American Lifestyle.Com

Manufactured In: United States

Units Affected: 2 products (13 boxes distributed domestically & 50 boxes distributed internationally to consumers; 3 boxes distributed domestically & 4 boxes distributed internationally to consumers.)

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

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