NDC 15631-0046

ARGENTUM OXYDATUM

Argentum Oxydatum

ARGENTUM OXYDATUM 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 Silver Oxide.

Product ID15631-0046_6cc53f83-dc7d-48d0-b604-f46cb7de5ee7
NDC15631-0046
Product TypeHuman Otc Drug
Proprietary NameARGENTUM OXYDATUM
Generic NameArgentum Oxydatum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-07
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameSILVER OXIDE
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0046-0

100 PELLET in 1 PACKAGE (15631-0046-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0046-3 [15631004603]

ARGENTUM OXYDATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-12

NDC 15631-0046-4 [15631004604]

ARGENTUM OXYDATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-12

NDC 15631-0046-2 [15631004602]

ARGENTUM OXYDATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-12

NDC 15631-0046-1 [15631004601]

ARGENTUM OXYDATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-12

NDC 15631-0046-5 [15631004605]

ARGENTUM OXYDATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-12

NDC 15631-0046-0 [15631004600]

ARGENTUM OXYDATUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-12

Drug Details

Active Ingredients

IngredientStrength
SILVER OXIDE3 [hp_X]/1

OpenFDA Data

SPL SET ID:c6645e78-a493-4cfa-b3e6-b932901d0ea0
Manufacturer
UNII

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