NDC 15631-0308

NATRUM CARBONICUM

Natrum Carbonicum

NATRUM CARBONICUM 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 Sodium Carbonate.

Product ID15631-0308_a199ba61-0bf8-50e8-e053-2995a90ab90c
NDC15631-0308
Product TypeHuman Otc Drug
Proprietary NameNATRUM CARBONICUM
Generic NameNatrum Carbonicum
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 NameSODIUM CARBONATE
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0308-0

100 PELLET in 1 PACKAGE (15631-0308-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0308-4 [15631030804]

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

NDC 15631-0308-0 [15631030800]

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

NDC 15631-0308-2 [15631030802]

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

NDC 15631-0308-5 [15631030805]

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

NDC 15631-0308-3 [15631030803]

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

NDC 15631-0308-1 [15631030801]

NATRUM CARBONICUM 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
SODIUM CARBONATE1 [hp_X]/1

OpenFDA Data

SPL SET ID:dd88d7d7-4051-4eca-9efc-10a941660c8c
Manufacturer
UNII

NDC Crossover Matching brand name "NATRUM CARBONICUM" or generic name "Natrum Carbonicum"

NDCBrand NameGeneric Name
0220-3531Natrum carbonicumSODIUM CARBONATE
0220-3532Natrum carbonicumSODIUM CARBONATE
0220-3533Natrum carbonicumSODIUM CARBONATE
0220-3534Natrum carbonicumSODIUM CARBONATE
0220-3535Natrum carbonicumSODIUM CARBONATE
0220-3536Natrum carbonicumSODIUM CARBONATE
0220-3537Natrum carbonicumSODIUM CARBONATE
0220-3538Natrum carbonicumSODIUM CARBONATE
0220-3577Natrum carbonicumSODIUM CARBONATE
15631-0308NATRUM CARBONICUMNATRUM CARBONICUM
15631-0638NATRUM CARBONICUMNATRUM CARBONICUM
37662-1870Natrum CarbonicumNatrum Carbonicum
37662-1871Natrum CarbonicumNatrum Carbonicum
37662-1872Natrum CarbonicumNatrum Carbonicum
37662-1873Natrum CarbonicumNatrum Carbonicum
37662-1874Natrum CarbonicumNatrum Carbonicum
37662-1875Natrum CarbonicumNatrum Carbonicum
37662-1876Natrum CarbonicumNatrum Carbonicum
37662-1877Natrum CarbonicumNatrum Carbonicum
62106-5189NATRUM CARBONICUMSodium carbonate
68428-524Natrum carbonicumSODIUM CARBONATE
71919-482Natrum carbonicumSODIUM CARBONATE

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