NDC 15631-0335

PHOSPHORICUM ACIDUM

Phosphoricum Acidum

PHOSPHORICUM 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 Phosphoric Acid.

Product ID15631-0335_a19b0736-8f1d-c458-e053-2995a90a36d0
NDC15631-0335
Product TypeHuman Otc Drug
Proprietary NamePHOSPHORICUM ACIDUM
Generic NamePhosphoricum Acidum
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 NamePHOSPHORIC ACID
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0335-0

100 PELLET in 1 PACKAGE (15631-0335-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0335-1 [15631033501]

PHOSPHORICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0335-5 [15631033505]

PHOSPHORICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0335-2 [15631033502]

PHOSPHORICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0335-3 [15631033503]

PHOSPHORICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0335-0 [15631033500]

PHOSPHORICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

NDC 15631-0335-4 [15631033504]

PHOSPHORICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-24

Drug Details

Active Ingredients

IngredientStrength
PHOSPHORIC ACID3 [hp_X]/1

OpenFDA Data

SPL SET ID:b9fa6434-1d71-4d40-b275-b5b2fbb126c1
Manufacturer
UNII

NDC Crossover Matching brand name "PHOSPHORICUM ACIDUM" or generic name "Phosphoricum Acidum"

NDCBrand NameGeneric Name
0220-3993Phosphoricum acidumPHOSPHORIC ACID
0220-3994Phosphoricum acidumPHOSPHORIC ACID
0220-4000Phosphoricum acidumPHOSPHORIC ACID
0220-4007Phosphoricum acidumPHOSPHORIC ACID
0220-4008Phosphoricum acidumPHOSPHORIC ACID
0220-4009Phosphoricum acidumPHOSPHORIC ACID
0220-4010Phosphoricum acidumPHOSPHORIC ACID
0220-4011Phosphoricum acidumPHOSPHORIC ACID
0220-4012Phosphoricum acidumPHOSPHORIC ACID
15631-0335PHOSPHORICUM ACIDUMPHOSPHORICUM ACIDUM
15631-0651PHOSPHORICUM ACIDUMPHOSPHORICUM ACIDUM
62106-4808PHOSPHORICUM ACIDUMOrthophosphoric acid
68428-560Phosphoricum acidumPHOSPHORIC ACID
71919-530Phosphoricum acidumPHOSPHORIC ACID
79718-1012Phosphoricum AcidumPhosphoricum Acidum
10893-110NaturasilPhosphoricum Acidum
10893-120NaturasilPhosphoricum Acidum
69152-1055Phosphoricum acidum 200CPhosphoricum acidum
69152-1220Phosphoricum acidum 6CPhosphoricum acidum

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