Reference Source

PAU YUEN TONG & CO · 66-41 · SOUTH AFRICA

For PAU YUEN TONG & CO · 66-41 · SOUTH AFRICA, import alert is 66-41; import alert name is Detention Without Physical Examination of Unapproved New Drugs Promoted In The U.S; country is SOUTH AFRICA; product is The Brush; product code is 66 V - - 99 Miscellaneous Patent Medicines, Etc; date published is 10/01/2024; address is 16 Okiep Street , Pretoria, Gauteng SOUTH AFRICA, verified against its source on 2026-09-16.

Firm
PAU YUEN TONG & CO verified
Import alert
66-41
Import alert name
Detention Without Physical Examination of Unapproved New Drugs Promoted In The U.S.
Country
SOUTH AFRICA verified
Address
16 Okiep Street , Pretoria, Gauteng SOUTH AFRICA verified
Date published
10/01/2024 verified
Product code
66 V - - 99 Miscellaneous Patent Medicines, Etc. verified
Product
The Brush verified
FDA notes
The product is not generally recognized as safe and effective for the above referenced uses and therefore, the product is a "new drug” under section 201(p) of the Act [21 U.S.C. § 321(p)]. New drugs may not be legally marketed in the U.S. without prior approval from the FDA as described in section 505(a) of the Act [21 U.S.C. § 355(a)]. There is no FDA-approved application in effect for “THE BRUSH.” Therefore, the article is subject to refusal of admission pursuant to section 801(a)(3) of the Federal Food, Drug and Cosmetic Act (the Act) in that it appears to be a new drug within the meaning of Section 201(p) of the Act without an effective new drug application (NDA) [Unapproved New Drug, Section 505(a)]. verified
Sourceaccessdata.fda.gov
Verified
Review by
DatasetFDA import alert red lists: firms subject to detention without physical examination

What the source says

PAU YUEN TONG & CO Date Published : 10/01/2024 16 Okiep Street , Pretoria, Gauteng SOUTH AFRICA 66 V - - 99 Miscellaneous Patent Medicines, Etc. Date Published: 10/01/2024 Desc: The Brush Notes: The product is not generally recognized as safe and effective for the above referenced uses and therefore, the product is a "new drug” under section 201(p) of the Act [21 U.S.C. § 321(p)]. New drugs may not be legally marketed in the U.S. without prior approval from the FDA as described in section 505(a) of the Act [21 U.S.C. § 355(a)]. There is no FDA-approved application in effect for “THE BRUSH.” Therefore, the article is subject to refusal of admission pursuant to section 801(a)(3) of the Federal Food, Drug and Cosmetic Act (the Act) in that it appears to be a new drug within the meaning of Section 201(p) of the Act without an effective new drug application (NDA) [Unapproved New Drug, Section 505(a)].

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

Source

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