NDC 15631-0652

PHOSPHORUS

Phosphorus

PHOSPHORUS 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 Phosphorus.

Product ID15631-0652_d5049f67-3cc8-4c8a-b4d1-fb2dcab6f755
NDC15631-0652
Product TypeHuman Otc Drug
Proprietary NamePHOSPHORUS
Generic NamePhosphorus
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2015-12-26
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NamePHOSPHORUS
Active Ingredient Strength4 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0652-2

50 TABLET in 1 CONTAINER (15631-0652-2)
Marketing Start Date2015-12-26
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0652-6 [15631065206]

PHOSPHORUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0652-7 [15631065207]

PHOSPHORUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0652-4 [15631065204]

PHOSPHORUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0652-1 [15631065201]

PHOSPHORUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0652-2 [15631065202]

PHOSPHORUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0652-5 [15631065205]

PHOSPHORUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0652-3 [15631065203]

PHOSPHORUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

NDC 15631-0652-0 [15631065200]

PHOSPHORUS TABLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-12-26
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
PHOSPHORUS4 [hp_X]/1

OpenFDA Data

SPL SET ID:bb0f42e3-56b1-4675-8368-add31b220df0
Manufacturer
UNII
UPC Code
  • 8907460005526
  • NDC Crossover Matching brand name "PHOSPHORUS" or generic name "Phosphorus"

    NDCBrand NameGeneric Name
    0220-4004PhosphorusPHOSPHORUS
    0220-4015PhosphorusPHOSPHORUS
    0220-4019PhosphorusPHOSPHORUS
    0220-4023PhosphorusPHOSPHORUS
    0220-4024PhosphorusPHOSPHORUS
    0220-4027PhosphorusPHOSPHORUS
    0220-4031PhosphorusPHOSPHORUS
    0220-4032PhosphorusPHOSPHORUS
    0220-4035PhosphorusPHOSPHORUS
    0220-4036PhosphorusPHOSPHORUS
    0220-4040PhosphorusPHOSPHORUS
    0360-0301PHOSPHORUSPHOSPHORUS
    0360-0304PHOSPHORUSPHOSPHORUS
    0360-0305PHOSPHORUSPHOSPHORUS
    15631-0336PHOSPHORUSPHOSPHORUS
    15631-0652PHOSPHORUSPHOSPHORUS
    44911-0155PhosphorusPhosphorus
    44911-0175PhosphorusPhosphorus
    53645-1170PhosphorusPhosphorus
    53645-1171PhosphorusPhosphorus
    54973-0622PHOSPHORUSphosphorus
    54973-2932PHOSPHORUSphosphorus
    55714-6417PhosphorusPhosphorus
    60512-1036PHOSPHORUSPHOSPHORUS
    62106-5249PHOSPHORUSPhosphorus
    63083-7130PhosphorusPhosphorus
    68428-561PhosphorusPhosphorus
    71919-531PhosphorusPhosphorus
    76472-1156PhosphorusPhosphorus
    64117-984Cough Sore ThroatPHOSPHORUS
    68428-063Phosphorus Kit RefillPHOSPHORUS
    68428-113Phosphorus Kit RefillPHOSPHORUS

    Trademark Results [PHOSPHORUS]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    PHOSPHORUS
    PHOSPHORUS
    90623821 not registered Live/Pending
    Phosphorus Cybersecurity Inc.
    2021-04-05
    PHOSPHORUS
    PHOSPHORUS
    87083408 5215288 Live/Registered
    PHOSPHORUS, INC.
    2016-06-24
    PHOSPHORUS
    PHOSPHORUS
    85479035 not registered Dead/Abandoned
    White Oak Technologies, Inc.
    2011-11-22

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