NDC 15631-0336

PHOSPHORUS

Phosphorus

PHOSPHORUS 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 Phosphorus.

Product ID15631-0336_a1bbca25-9916-f171-e053-2a95a90a09f1
NDC15631-0336
Product TypeHuman Otc Drug
Proprietary NamePHOSPHORUS
Generic NamePhosphorus
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-12
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NamePHOSPHORUS
Active Ingredient Strength4 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0336-0

100 PELLET in 1 PACKAGE (15631-0336-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0336-0 [15631033600]

PHOSPHORUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0336-3 [15631033603]

PHOSPHORUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0336-2 [15631033602]

PHOSPHORUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0336-1 [15631033601]

PHOSPHORUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0336-4 [15631033604]

PHOSPHORUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

NDC 15631-0336-5 [15631033605]

PHOSPHORUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-26

Drug Details

Active Ingredients

IngredientStrength
PHOSPHORUS4 [hp_X]/1

OpenFDA Data

SPL SET ID:21fa8f76-af69-4812-b291-a6bdeffbfd00
Manufacturer
UNII

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

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