Reference Source

Japanese Mayo Kaisha Pharmacy Export Ltd · 66-41 · JAPAN

For Japanese Mayo Kaisha Pharmacy Export Ltd, import alert is 66-41; country is JAPAN; import alert name is Detention Without Physical Examination of Unapproved New Drugs Promoted In The U.S; product is Stree Overload Capsules; product code is 66 V - - 99 Miscellaneous Patent Medicines, Etc; date published is 09/30/2009; address is 16F, Bi Fu Tong Bldg No. 88 , Gao Shi Da Dao , Tokyo, JAPAN, verified against its source on 2026-10-01.

Firm
Japanese Mayo Kaisha Pharmacy Export Ltd verified
Import alert
66-41
Import alert name
Detention Without Physical Examination of Unapproved New Drugs Promoted In The U.S.
Country
JAPAN verified
Address
16F, Bi Fu Tong Bldg No. 88 , Gao Shi Da Dao , Tokyo, JAPAN verified
Date published
09/30/2009 verified
Product code
66 V - - 99 Miscellaneous Patent Medicines, Etc. verified
Product
Stree Overload Capsules verified
FDA notes
This product insert claims that the capsules can treat male impotence; prostatitis; and sexual impotence caused by diabetes. The product is also claimed to be superior to the erectile dysfunction drugs Viagra and Cialis. 8/10/2009 verified
Sourceaccessdata.fda.gov
Verified
Review by
DatasetFDA import alert red lists: firms subject to detention without physical examination

What the source says

Japanese Mayo Kaisha Pharmacy Export Ltd Date Published : 09/30/2009 16F, Bi Fu Tong Bldg No. 88 , Gao Shi Da Dao , Tokyo, JAPAN

— accessdata.fda.gov, retrieved 2026-09-15

Where each value comes from

The values above are stated away from the sentence quoted with the answer, so the passage that states them is shown here too.

Product code, Product and FDA notes

66 V - - 99 Miscellaneous Patent Medicines, Etc. Date Published: 09/13/2019 Desc: Stree Overload Capsules Notes: This product insert claims that the capsules can treat male impotence; prostatitis; and sexual impotence caused by diabetes. The product is also claimed to be superior to the erectile dysfunction drugs Viagra and Cialis. 8/10/2009

— all from accessdata.fda.gov, retrieved 2026-09-15

Source

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