NDC 63083-8101

Aventurine 8101

Aventurine

Aventurine 8101 is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Professional Complementary Health Formulas. The primary component is Silicon Dioxide.

Product ID63083-8101_185cee1f-c774-4fc7-8848-fd39fd26b555
NDC63083-8101
Product TypeHuman Otc Drug
Proprietary NameAventurine 8101
Generic NameAventurine
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date1984-08-15
Marketing CategoryUNAPPROVED HOMEOPATHIC /
Labeler NameProfessional Complementary Health Formulas
Substance NameSILICON DIOXIDE
Active Ingredient Strength6 [hp_X]/59mL
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 63083-8101-2

59 mL in 1 BOTTLE, DROPPER (63083-8101-2)
Marketing Start Date1985-08-15
NDC Exclude FlagN
Sample Package?N

Drug Details


Trademark Results [Aventurine]

Mark Image

Registration | Serial
Company
Trademark
Application Date
AVENTURINE
AVENTURINE
98630095 not registered Live/Pending
Aventurine Studio One LLC
2024-07-02
AVENTURINE
AVENTURINE
90137143 not registered Live/Pending
Mitchell, Nicole D
2020-08-25
AVENTURINE
AVENTURINE
90062907 not registered Live/Pending
Aventurine Capital Management LLC
2020-07-20
AVENTURINE
AVENTURINE
77848394 3824168 Dead/Cancelled
Kowdley, Sandhya
2009-10-14

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.