NDC 15631-0254

KALI SULPHURICUM

Kali Sulphuricum

KALI SULPHURICUM 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 Sulfate.

Product ID15631-0254_a1829e38-f097-5590-e053-2a95a90aacfa
NDC15631-0254
Product TypeHuman Otc Drug
Proprietary NameKALI SULPHURICUM
Generic NameKali Sulphuricum
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 SULFATE
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0254-0

100 PELLET in 1 PACKAGE (15631-0254-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0254-0 [15631025400]

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

NDC 15631-0254-1 [15631025401]

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

NDC 15631-0254-3 [15631025403]

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

NDC 15631-0254-5 [15631025405]

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

NDC 15631-0254-2 [15631025402]

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

NDC 15631-0254-4 [15631025404]

KALI SULPHURICUM 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 SULFATE1 [hp_X]/1

OpenFDA Data

SPL SET ID:8bcb266a-f8d7-44b5-a6f0-2d5803497b19
Manufacturer
UNII

NDC Crossover Matching brand name "KALI SULPHURICUM" or generic name "Kali Sulphuricum"

NDCBrand NameGeneric Name
0220-2921Kali sulphuricumPOTASSIUM SULFATE
0220-2973Kali sulphuricumPOTASSIUM SULFATE
0220-2974Kali sulphuricumPOTASSIUM SULFATE
0220-2975Kali sulphuricumPOTASSIUM SULFATE
0220-2976Kali sulphuricumPOTASSIUM SULFATE
0220-2977Kali sulphuricumPOTASSIUM SULFATE
0220-2978Kali sulphuricumPOTASSIUM SULFATE
0220-2979Kali sulphuricumPOTASSIUM SULFATE
0360-0241KALI SULPHURICUMKALI SULPH
0360-0243KALI SULPHURICUMKALI SULPH
15631-0254KALI SULPHURICUMKALI SULPHURICUM
15631-0613KALI SULPHURICUMKALI SULPHURICUM
37662-2182Kali SulphuricumKali Sulphuricum
37662-2183Kali SulphuricumKali Sulphuricum
37662-2184Kali SulphuricumKali Sulphuricum
37662-2185Kali SulphuricumKali Sulphuricum
37662-2186Kali SulphuricumKali Sulphuricum
37662-2187Kali SulphuricumKali Sulphuricum
37662-2188Kali SulphuricumKali Sulphuricum
37662-2189Kali SulphuricumKali Sulphuricum
60512-8023KALI SULPHURICUMKALI SULPHURICUM
60512-8024KALI SULPHURICUMKALI SULPHURICUM
62106-5110KALI SULPHURICUMPotassium sulfate
63083-8007Kali SulphuricumKali Sulphuricum
68428-457Kali sulphuricumPOTASSIUM SULFATE
71753-8007Kali SulphuricumKali Sulphuricum
71919-389Kali sulphuricumPOTASSIUM SULFATE
71919-745KALI SULPHURICUMPOTASSIUM SULFATE
44911-0354Kali SulphKali Sulphuricum

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