NDC 15631-0056

ARTEMISIA VULGARIS

Artemisia Vulgaris

ARTEMISIA VULGARIS 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 Artemisia Vulgaris Root.

Product ID15631-0056_8a4c12fc-8eab-4b53-b897-8466b1fd7549
NDC15631-0056
Product TypeHuman Otc Drug
Proprietary NameARTEMISIA VULGARIS
Generic NameArtemisia Vulgaris
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-11
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameARTEMISIA VULGARIS ROOT
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0056-0

100 PELLET in 1 PACKAGE (15631-0056-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0056-4 [15631005604]

ARTEMISIA VULGARIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0056-2 [15631005602]

ARTEMISIA VULGARIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0056-5 [15631005605]

ARTEMISIA VULGARIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0056-0 [15631005600]

ARTEMISIA VULGARIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0056-1 [15631005601]

ARTEMISIA VULGARIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

NDC 15631-0056-3 [15631005603]

ARTEMISIA VULGARIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-17

Drug Details

Active Ingredients

IngredientStrength
ARTEMISIA VULGARIS ROOT1 [hp_X]/1

OpenFDA Data

SPL SET ID:eb466c60-7d59-4c5e-b1ee-c0d6ee53650f
Manufacturer
UNII

NDC Crossover Matching brand name "ARTEMISIA VULGARIS" or generic name "Artemisia Vulgaris"

NDCBrand NameGeneric Name
0220-0552Artemisia vulgarisARTEMISIA VULGARIS ROOT
15631-0056ARTEMISIA VULGARISARTEMISIA VULGARIS
60512-6516ARTEMISIA VULGARISARTEMISIA VULGARIS
63545-230Artemisia VulgarisArtemisia Vulgaris
63545-231Artemisia VulgarisArtemisia Vulgaris
63545-232Artemisia VulgarisArtemisia Vulgaris
63545-233Artemisia VulgarisArtemisia Vulgaris
63545-234Artemisia VulgarisArtemisia Vulgaris
63545-235Artemisia VulgarisArtemisia Vulgaris
63545-236Artemisia VulgarisArtemisia Vulgaris
63545-237Artemisia VulgarisArtemisia Vulgaris
63545-238Artemisia VulgarisArtemisia Vulgaris
68428-892Artemisia vulgarisARTEMISIA VULGARIS ROOT
71919-088Artemisia vulgarisARTEMISIA VULGARIS ROOT
69152-1574Artemisia vulgaris 1XArtemisia vulgaris
69152-1184Artemisia vulgaris 6CArtemisia vulgaris
22840-1348Common MugwortArtemisia vulgaris
22840-2340Common MugwortArtemisia vulgaris
22840-5314Common MugwortArtemisia vulgaris
49643-321Mugwort Sage PollenArtemisia vulgaris

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