NDC 15631-0292

MERCURIUS DULCIS

Mercurius Dulcis

MERCURIUS DULCIS 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 Calomel.

Product ID15631-0292_a1947eca-29b2-98d1-e053-2a95a90ad30b
NDC15631-0292
Product TypeHuman Otc Drug
Proprietary NameMERCURIUS DULCIS
Generic NameMercurius Dulcis
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-10
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameCALOMEL
Active Ingredient Strength6 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0292-0

100 PELLET in 1 PACKAGE (15631-0292-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0292-2 [15631029202]

MERCURIUS DULCIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0292-0 [15631029200]

MERCURIUS DULCIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0292-5 [15631029205]

MERCURIUS DULCIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0292-1 [15631029201]

MERCURIUS DULCIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0292-4 [15631029204]

MERCURIUS DULCIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0292-3 [15631029203]

MERCURIUS DULCIS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

Drug Details

Active Ingredients

IngredientStrength
CALOMEL6 [hp_X]/1

OpenFDA Data

SPL SET ID:172361e7-4029-4ad4-b3d9-5dfe2e1723ec
Manufacturer
UNII

NDC Crossover Matching brand name "MERCURIUS DULCIS" or generic name "Mercurius Dulcis"

NDCBrand NameGeneric Name
0220-3372Mercurius dulcisCALOMEL
0220-3373Mercurius dulcisCALOMEL
0220-3395Mercurius dulcisCALOMEL
15631-0292MERCURIUS DULCISMERCURIUS DULCIS
37662-1818Mercurius DulcisMercurius Dulcis
37662-1819Mercurius DulcisMercurius Dulcis
37662-1820Mercurius DulcisMercurius Dulcis
37662-1821Mercurius DulcisMercurius Dulcis
37662-1822Mercurius DulcisMercurius Dulcis
37662-1823Mercurius DulcisMercurius Dulcis
37662-1824Mercurius DulcisMercurius Dulcis
37662-1825Mercurius DulcisMercurius Dulcis
37662-1826Mercurius DulcisMercurius Dulcis
62106-5165MERCURIUS DULCISMild mercury chloride
68428-504Mercurius dulcisCALOMEL
71919-458Mercurius dulcisCALOMEL

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