NDC 15631-0174

ECHINACEA PURPUREA

Echinacea Purpurea

ECHINACEA PURPUREA is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Echinacea Purpurea.

Product ID15631-0174_33c19aa8-3fbd-4672-82e2-ffa0e9f66649
NDC15631-0174
Product TypeHuman Otc Drug
Proprietary NameECHINACEA PURPUREA
Generic NameEchinacea Purpurea
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-02
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameECHINACEA PURPUREA
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0174-0

100 PELLET in 1 PACKAGE (15631-0174-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0174-4 [15631017404]

ECHINACEA PURPUREA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

NDC 15631-0174-5 [15631017405]

ECHINACEA PURPUREA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

NDC 15631-0174-3 [15631017403]

ECHINACEA PURPUREA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

NDC 15631-0174-0 [15631017400]

ECHINACEA PURPUREA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

NDC 15631-0174-2 [15631017402]

ECHINACEA PURPUREA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

NDC 15631-0174-1 [15631017401]

ECHINACEA PURPUREA PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-19

Drug Details

Active Ingredients

IngredientStrength
ECHINACEA PURPUREA1 [hp_X]/1

OpenFDA Data

SPL SET ID:6b29c742-ed02-4537-8290-b71452f6aca7
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

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