NDC 15631-0178

EQUISETUM ARVENSE

Equisetum Arvense

EQUISETUM ARVENSE 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 Equisetum Arvense Top.

Product ID15631-0178_a11ad69a-1990-78e9-e053-2a95a90a8b84
NDC15631-0178
Product TypeHuman Otc Drug
Proprietary NameEQUISETUM ARVENSE
Generic NameEquisetum Arvense
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 NameEQUISETUM ARVENSE TOP
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0178-0

100 PELLET in 1 PACKAGE (15631-0178-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0178-0 [15631017800]

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

NDC 15631-0178-5 [15631017805]

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

NDC 15631-0178-3 [15631017803]

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

NDC 15631-0178-1 [15631017801]

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

NDC 15631-0178-2 [15631017802]

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

NDC 15631-0178-4 [15631017804]

EQUISETUM ARVENSE 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
EQUISETUM ARVENSE TOP1 [hp_X]/1

OpenFDA Data

SPL SET ID:808501d1-8e14-4f5d-a5a8-89a89c21eda5
Manufacturer
UNII

NDC Crossover Matching brand name "EQUISETUM ARVENSE" or generic name "Equisetum Arvense"

NDCBrand NameGeneric Name
0220-1892Equisetum arvenseEQUISETUM ARVENSE TOP
0220-1893Equisetum arvenseEQUISETUM ARVENSE TOP
15631-0178EQUISETUM ARVENSEEQUISETUM ARVENSE
68428-367Equisetum arvenseEQUISETUM ARVENSE TOP
71919-268Equisetum arvenseEQUISETUM ARVENSE TOP

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