NDC 15631-0035

ANTIMONIUM ARSENICICUM

Antimonium Arsenicicum

ANTIMONIUM ARSENICICUM 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 Antimony Arsenate.

Product ID15631-0035_9e3925c7-161c-4837-e053-2a95a90a2c6c
NDC15631-0035
Product TypeHuman Otc Drug
Proprietary NameANTIMONIUM ARSENICICUM
Generic NameAntimonium Arsenicicum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-06
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameANTIMONY ARSENATE
Active Ingredient Strength6 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0035-0

100 PELLET in 1 PACKAGE (15631-0035-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0035-3 [15631003503]

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

NDC 15631-0035-4 [15631003504]

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

NDC 15631-0035-5 [15631003505]

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

NDC 15631-0035-1 [15631003501]

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

NDC 15631-0035-2 [15631003502]

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

NDC 15631-0035-0 [15631003500]

ANTIMONIUM ARSENICICUM 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
ANTIMONY ARSENATE6 [hp_X]/1

OpenFDA Data

SPL SET ID:83ad2d19-677e-485c-9f19-8c7c681da3dd
Manufacturer
UNII

NDC Crossover Matching brand name "ANTIMONIUM ARSENICICUM" or generic name "Antimonium Arsenicicum"

NDCBrand NameGeneric Name
15631-0035ANTIMONIUM ARSENICICUMANTIMONIUM ARSENICICUM
68428-211Antimonium arsenicicumANTIMONY ARSENATE
71919-063Antimonium arsenicicumANTIMONY ARSENATE

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