NDC 15631-0422

SULPHURICUM ACIDUM

Sulphuricum Acidum

SULPHURICUM ACIDUM 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 Sulfuric Acid.

Product ID15631-0422_a1c3d04c-3af3-58bf-e053-2a95a90a7638
NDC15631-0422
Product TypeHuman Otc Drug
Proprietary NameSULPHURICUM ACIDUM
Generic NameSulphuricum Acidum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-11-03
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameSULFURIC ACID
Active Ingredient Strength6 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0422-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0422-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0422-4 [15631042204]

SULPHURICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0422-1 [15631042201]

SULPHURICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0422-0 [15631042200]

SULPHURICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0422-2 [15631042202]

SULPHURICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0422-3 [15631042203]

SULPHURICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

NDC 15631-0422-5 [15631042205]

SULPHURICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-27

Drug Details

Active Ingredients

IngredientStrength
SULFURIC ACID6 [hp_X]/1

OpenFDA Data

SPL SET ID:fdaf5ac7-47e6-4bfe-8cb2-768ed3c6815e
Manufacturer
UNII

NDC Crossover Matching brand name "SULPHURICUM ACIDUM" or generic name "Sulphuricum Acidum"

NDCBrand NameGeneric Name
0220-4841Sulphuricum acidumSULFURIC ACID
0220-4846Sulphuricum acidumSULFURIC ACID
0220-4847Sulphuricum acidumSULFURIC ACID
0220-4860Sulphuricum acidumSULFURIC ACID
0220-4861Sulphuricum acidumSULFURIC ACID
15631-0422SULPHURICUM ACIDUMSULPHURICUM ACIDUM
68428-657Sulphuricum acidumSULFURIC ACID
71919-654SULPHURICUM ACIDUMSulfuric acid

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