NDC 15631-0251

KALI MURIATICUM

Kali Muriaticum

KALI MURIATICUM 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 Potassium Chloride.

Product ID15631-0251_954003b2-879d-4819-971c-9c84123cad6f
NDC15631-0251
Product TypeHuman Otc Drug
Proprietary NameKALI MURIATICUM
Generic NameKali Muriaticum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-05
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NamePOTASSIUM CHLORIDE
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0251-0

100 PELLET in 1 PACKAGE (15631-0251-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0251-5 [15631025105]

KALI MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0251-4 [15631025104]

KALI MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0251-0 [15631025100]

KALI MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0251-1 [15631025101]

KALI MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0251-3 [15631025103]

KALI MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

NDC 15631-0251-2 [15631025102]

KALI MURIATICUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-23

Drug Details

Active Ingredients

IngredientStrength
POTASSIUM CHLORIDE1 [hp_X]/1

OpenFDA Data

SPL SET ID:b70cbfef-2c00-4e13-aa88-c411c5261230
Manufacturer
UNII

NDC Crossover Matching brand name "KALI MURIATICUM" or generic name "Kali Muriaticum"

NDCBrand NameGeneric Name
0220-2891Kali muriaticumPOTASSIUM CHLORIDE
0220-2951Kali muriaticumPOTASSIUM CHLORIDE
0220-2952Kali muriaticumPOTASSIUM CHLORIDE
0220-2953Kali muriaticumPOTASSIUM CHLORIDE
0220-2954Kali muriaticumPOTASSIUM CHLORIDE
0220-2955Kali muriaticumPOTASSIUM CHLORIDE
0220-2956Kali muriaticumPOTASSIUM CHLORIDE
0220-2957Kali muriaticumPOTASSIUM CHLORIDE
0220-2958Kali muriaticumPOTASSIUM CHLORIDE
0220-2959Kali muriaticumPOTASSIUM CHLORIDE
0360-0233KALI MURIATICUMKALI MUR
0360-0235KALI MURIATICUMKALI MUR
15631-0251KALI MURIATICUMKALI MURIATICUM
15631-0611KALI MURIATICUMKALI MURIATICUM
37662-0883Kali MuriaticumKali Muriaticum
37662-0884Kali MuriaticumKali Muriaticum
37662-0885Kali MuriaticumKali Muriaticum
37662-0886Kali MuriaticumKali Muriaticum
37662-0887Kali MuriaticumKali Muriaticum
37662-0888Kali MuriaticumKali Muriaticum
37662-0889Kali MuriaticumKali Muriaticum
37662-0890Kali MuriaticumKali Muriaticum
54973-3105KALI MURIATICUMpotassium chloride
54973-5224KALI MURIATICUMpotassium chloride
55714-6297Kali muriaticumKali muriaticum
60512-8019KALI MURIATICUMKALI MURIATICUM
60512-8020KALI MURIATICUMKALI MURIATICUM
62106-5098KALI MURIATICUMPotassium chloride
68428-454Kali muriaticumPOTASSIUM CHLORIDE
71753-8005Kali MuriaticumKali Muriaticum
71919-384Kali muriaticumPOTASSIUM CHLORIDE
71919-747Kali muriaticumPOTASSIUM CHLORIDE
44911-0166Kali MurKali Muriaticum

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