• 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 MQ9-0135608-8/6/1/A


Manufacturer FEI3007140468
Manufacturer NameDabur India Ltd  
Manufacturer Address line 1Village Billanwali Lavana, Baddi  
Manufacturer Address line 2Distt Solan  
Manufacturer's CityBaddi  
Manufacturer Province/StateIN-HP  
Manufacturer Country/AreaIndia  
Product Code53IG01  
Importer's Product DescriptionTOOTHPASTE  
Refusal Date31-Jan-2013  
FDA DistrictLOS-DO  
Entry/doc/line/sfx MQ9-0135608-8/6/1/A
FDA Sample AnalysisNo  
FDA Record of Private Lab Sample Analysis No  
Charge(s)
Violation Code Section Charge Statement
DIRSEXMPT   502(f)(1), 801(a)(3); MISBRANDING   The article appears to lack adequate directions for use, and the article does not appear to be exempt from such requirements.  
UNAPPROVED   505(a), 801(a)(3); UNAPPROVED NEW DRUG   The article appears to be a new drug without an approved new drug application.  
-
-