NDC 15631-0003

ABSINTHIUM

Absinthium

ABSINTHIUM 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 Wormwood.

Product ID15631-0003_565d381e-001e-40f0-83c0-6f0349eacefa
NDC15631-0003
Product TypeHuman Otc Drug
Proprietary NameABSINTHIUM
Generic NameAbsinthium
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-08-28
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameWORMWOOD
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0003-0

100 PELLET in 1 PACKAGE (15631-0003-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0003-0 [15631000300]

ABSINTHIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0003-3 [15631000303]

ABSINTHIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0003-4 [15631000304]

ABSINTHIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0003-1 [15631000301]

ABSINTHIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0003-2 [15631000302]

ABSINTHIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0003-5 [15631000305]

ABSINTHIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

Drug Details

Active Ingredients

IngredientStrength
WORMWOOD3 [hp_X]/1

OpenFDA Data

SPL SET ID:44566d0e-6d96-44fa-9f22-604628a868b2
Manufacturer
UNII

NDC Crossover Matching brand name "ABSINTHIUM" or generic name "Absinthium"

NDCBrand NameGeneric Name
0220-0018AbsinthiumWORMWOOD
15631-0003ABSINTHIUMABSINTHIUM
60512-6439ABSINTHIUMABSINTHIUM
63545-258AbsinthiumAbsinthium
63545-717AbsinthiumAbsinthium
63545-718AbsinthiumAbsinthium
63545-719AbsinthiumAbsinthium
63545-720AbsinthiumAbsinthium
63545-721AbsinthiumAbsinthium
63545-722AbsinthiumAbsinthium
68428-174AbsinthiumAbsinthium
71919-004AbsinthiumAbsinthium
63545-723AbsinthiumAbsinthium

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