NDC 60512-6651

ECHINACEA PURPUREA

Echinacea Purpurea

ECHINACEA PURPUREA is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Homeolab Usa Inc.. The primary component is Echinacea Purpurea.

Product ID60512-6651_72bfae31-b7e6-4ca2-87d4-d7e54efa9b18
NDC60512-6651
Product TypeHuman Otc Drug
Proprietary NameECHINACEA PURPUREA
Generic NameEchinacea Purpurea
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2013-11-18
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameHOMEOLAB USA INC.
Substance NameECHINACEA PURPUREA
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 60512-6651-1

80 PELLET in 1 TUBE (60512-6651-1)
Marketing Start Date2013-11-18
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 60512-6651-1 [60512665101]

ECHINACEA PURPUREA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-11-18
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ECHINACEA PURPUREA1 [hp_X]/1

OpenFDA Data

SPL SET ID:6251215d-19d1-4736-88de-0f7e20d2f13d
Manufacturer
UNII

NDC Crossover Matching brand name "ECHINACEA PURPUREA" or generic name "Echinacea Purpurea"

NDCBrand NameGeneric Name
0220-1856Echinacea purpureaECHINACEA PURPUREA
15631-0174ECHINACEA PURPUREAECHINACEA PURPUREA
60512-6651ECHINACEA PURPUREAECHINACEA PURPUREA
68428-362Echinacea purpureaECHINACEA PURPUREA
71919-263Echinacea purpureaECHINACEA PURPUREA
62106-1183ECHINASYREchinacea purpurea

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