NDC 15631-0692

SULPHUR

Sulphur

SULPHUR 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 Sulfur.

Product ID15631-0692_6de71700-bc3d-4889-be61-fa15d57d8232
NDC15631-0692
Product TypeHuman Otc Drug
Proprietary NameSULPHUR
Generic NameSulphur
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-27
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 15631-0692-2

50 TABLET in 1 CONTAINER (15631-0692-2)
Marketing Start Date2015-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0692-7 [15631069207]

SULPHUR TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0692-0 [15631069200]

SULPHUR TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0692-2 [15631069202]

SULPHUR TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0692-6 [15631069206]

SULPHUR TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0692-3 [15631069203]

SULPHUR TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0692-4 [15631069204]

SULPHUR TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0692-5 [15631069205]

SULPHUR TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

NDC 15631-0692-1 [15631069201]

SULPHUR TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-27
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
SULFUR1 [hp_X]/1

OpenFDA Data

SPL SET ID:93f9d1ab-d6f8-4df3-a990-af633aa956de
Manufacturer
UNII
UPC Code
  • 8907460005526

    • 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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