The Sun Studio · 66-41 · UNITED KINGDOM
For The Sun Studio · 66-41 · UNITED KINGDOM, import alert is 66-41; import alert name is Detention Without Physical Examination of Unapproved New Drugs Promoted In The U.S; country is UNITED KINGDOM; product is Detox Food Patches (Bodytox); product code is 66 V D K 99 Miscellaneous Patent Medicines, Etc., Human - Rx/Combination Ingredient, Sterile Liquid; date published is 09/30/2009; address is 113 Newland Street , Withamwitham, UNITED KINGDOM, verified against its source on 2026-09-16.
- Firm
- The Sun Studio verified
- Import alert
- 66-41
- Import alert name
- Detention Without Physical Examination of Unapproved New Drugs Promoted In The U.S.
- Country
- UNITED KINGDOM verified
- Address
- 113 Newland Street , Withamwitham, UNITED KINGDOM verified
- Date published
- 09/30/2009 verified
- Product code
- 66 V D K 99 Miscellaneous Patent Medicines, Etc., Human - Rx/Combination Ingredient, Sterile Liquid verified
- Product
- Detox Food Patches (Bodytox) verified
- FDA notes
- CDER has determined that this product is an unapproved new drug based on labeling which suggests that the patch be placed on parts of the body to positively affect bodily structures and functions. CDER is not aware of any scientific evidence that this product is safe and effective for the uses suggested in its labeling. CDER has also determined that this product lacks adequate directions for use. 8/10/09 verified
What the source says
The Sun Studio Date Published : 09/30/2009 113 Newland Street , Withamwitham, UNITED KINGDOM 66 V D K 99 Miscellaneous Patent Medicines, Etc., Human - Rx/Combination Ingredient, Sterile Liquid Date Published: 09/30/2009 Desc: Detox Food Patches (Bodytox) Notes: CDER has determined that this product is an unapproved new drug based on labeling which suggests that the patch be placed on parts of the body to positively affect bodily structures and functions. CDER is not aware of any scientific evidence that this product is safe and effective for the uses suggested in its labeling. CDER has also determined that this product lacks adequate directions for use. 8/10/09
— accessdata.fda.gov, retrieved 2026-09-15
Source
- accessdata.fda.govhttps://www.accessdata.fda.gov/cms_ia/importalert_190.html
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