NDC 15631-0638

NATRUM CARBONICUM

Natrum Carbonicum

NATRUM CARBONICUM is a Oral Tablet 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 ID15631-0638_561e3182-da75-4e18-83da-6e240d0f74d4
NDC15631-0638
Product TypeHuman Otc Drug
Proprietary NameNATRUM CARBONICUM
Generic NameNatrum Carbonicum
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-26
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 FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0638-0

1 TABLET in 1 BLISTER PACK (15631-0638-0)
Marketing Start Date2015-12-26
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0638-1 [15631063801]

NATRUM CARBONICUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0638-2 [15631063802]

NATRUM CARBONICUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0638-4 [15631063804]

NATRUM CARBONICUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0638-3 [15631063803]

NATRUM CARBONICUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0638-7 [15631063807]

NATRUM CARBONICUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0638-6 [15631063806]

NATRUM CARBONICUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0638-5 [15631063805]

NATRUM CARBONICUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0638-0 [15631063800]

NATRUM CARBONICUM TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
SODIUM CARBONATE1 [hp_X]/1

OpenFDA Data

SPL SET ID:600728b2-a019-41b1-88d6-f2283ada550d
Manufacturer
UNII
UPC Code
  • 8907460005526
  • 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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