Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Import Refusal Report
  • Print
  • Share
  • E-mail
-

Refusal Details as Recorded in OASIS by FDA

for Refusal ED5-0046189-9/6/1

Manufacturer FEI3006632871
Manufacturer NameTopline Exim Inc.  
Manufacturer Address line 11002 Abhijeet-2  
Manufacturer Address line 2Mithakhali Six Roads  
Manufacturer's CityAhmedabad  
Manufacturer Province/State  
Manufacturer Country/AreaIndia  
Product Code53GH04  
Importer's Product DescriptionHENNA  
Refusal Date14-Sep-2012  
FDA DistrictNWE-DO  
Entry/doc/line/sfx ED5-0046189-9/6/1
FDA Sample AnalysisNo  
FDA Record of Private Lab Sample Analysis No  
Charge(s)
Violation Code Section Charge Statement
COSM COLOR   601(e), 801(a)(3); ADULTERATION   The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a color additive which is unsafe within the meaning of Section 721(a) which renders it adulterated under Section 601(e).  
CSTIC LBLG   602(a) and/or (b), and/or (c), 801(a)(3); MISBRANDING   The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.  
LABELING   Section 4(a); 801(a)(3) Misbranding   The article appears in violation of FPLA because of its placement, form and/or contents statement.  
-
-