NDC 15631-0420

SULPHUR

Sulphur

SULPHUR 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 Sulfur.

Product ID15631-0420_3c1405b6-9967-408b-bc62-e648436b7718
NDC15631-0420
Product TypeHuman Otc Drug
Proprietary NameSULPHUR
Generic NameSulphur
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 NameSULFUR
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0420-0

100 PELLET in 1 VIAL, SINGLE-DOSE (15631-0420-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0420-5 [15631042005]

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

NDC 15631-0420-3 [15631042003]

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

NDC 15631-0420-0 [15631042000]

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

NDC 15631-0420-4 [15631042004]

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

NDC 15631-0420-2 [15631042002]

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

NDC 15631-0420-1 [15631042001]

SULPHUR 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
SULFUR1 [hp_X]/1

OpenFDA Data

SPL SET ID:61a36a56-4e62-4721-81fb-ee8dcd08b4d8
Manufacturer
UNII

NDC Crossover Matching brand name "SULPHUR" or generic name "Sulphur"

NDCBrand NameGeneric Name
0220-4813SulphurSULFUR
0220-4816SulphurSULFUR
0220-4817SulphurSULFUR
0220-4820SulphurSULFUR
0220-4821SulphurSULFUR
0220-4823SulphurSULFUR
0220-4826SulphurSULFUR
0220-4827SulphurSULFUR
0220-4828SulphurSULFUR
0220-4829SulphurSULFUR
0220-4830SulphurSULFUR
0220-4831SulphurSULFUR
0360-0368SULPHURSULPHOR
0360-0369SULPHURSULPHUR
10191-1578SULPHURSULFUR
10191-1585SULPHURSULFUR
10191-1587SULPHURSULFUR
10191-1589SULPHURSULFUR
15631-0420SULPHURSULPHUR
15631-0692SULPHURSULPHUR
15631-2322SULPHURSULPHUR
37662-2313SulphurSulphur
37662-2314SulphurSulphur
37662-2315SulphurSulphur
37662-2316SulphurSulphur
37662-2317SulphurSulphur
37662-2318SulphurSulphur
37662-2319SulphurSulphur
37662-2320SulphurSulphur
37662-2321SulphurSulphur
44911-0394SulphurSulphur
54973-0627SULPHURSULFUR
54973-2927SULPHURSULFUR
55714-6516SulphurSulphur
68428-655SulphurSulphur
60512-1047SULPHURSULPHUR
62106-5316SULPHURSULPHUR
76472-1165SULPHURSULPHUR
55714-7516SulphurSulphur
0295-7300ProsaceaSulphur
52389-173ProsaceaSulphur
43406-0472Sulphur 30CSulphur
51439-004Treatment 101Sulphur

Trademark Results [SULPHUR]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SULPHUR
SULPHUR
79280963 not registered Live/Pending
H Sulphur Corp.
2020-01-07
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