NDC 15631-0325

OXALICUM ACIDUM

Oxalicum Acidum

OXALICUM 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 Oxalic Acid Dihydrate.

Product ID15631-0325_94ec0897-38d9-4296-a7f6-51a6cedfe312
NDC15631-0325
Product TypeHuman Otc Drug
Proprietary NameOXALICUM ACIDUM
Generic NameOxalicum Acidum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-09-10
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameOXALIC ACID DIHYDRATE
Active Ingredient Strength6 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0325-0

100 PELLET in 1 PACKAGE (15631-0325-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0325-5 [15631032505]

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

NDC 15631-0325-0 [15631032500]

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

NDC 15631-0325-4 [15631032504]

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

NDC 15631-0325-2 [15631032502]

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

NDC 15631-0325-1 [15631032501]

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

NDC 15631-0325-3 [15631032503]

OXALICUM 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
OXALIC ACID DIHYDRATE6 [hp_X]/1

OpenFDA Data

SPL SET ID:568ccc95-8195-4dc9-baad-8df55a4571bf
Manufacturer
UNII

NDC Crossover Matching brand name "OXALICUM ACIDUM" or generic name "Oxalicum Acidum"

NDCBrand NameGeneric Name
0220-3840Oxalicum acidumOXALIC ACID DIHYDRATE
0220-3842Oxalicum acidumOXALIC ACID DIHYDRATE
15631-0325OXALICUM ACIDUMOXALICUM ACIDUM
68428-549Oxalicum acidumOXALIC ACID DIHYDRATE
71919-513Oxalicum acidumOXALIC ACID DIHYDRATE

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