NDC 15631-0201

GALLICUM ACIDUM

Gallicum Acidum

GALLICUM 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 Gallic Acid Monohydrate.

Product ID15631-0201_6fc6f347-6455-485c-92f4-50ec810e79d5
NDC15631-0201
Product TypeHuman Otc Drug
Proprietary NameGALLICUM ACIDUM
Generic NameGallicum Acidum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-02
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameGALLIC ACID MONOHYDRATE
Active Ingredient Strength2 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0201-0

100 PELLET in 1 PACKAGE (15631-0201-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0201-2 [15631020102]

GALLICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0201-4 [15631020104]

GALLICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0201-0 [15631020100]

GALLICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0201-5 [15631020105]

GALLICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0201-3 [15631020103]

GALLICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0201-1 [15631020101]

GALLICUM ACIDUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

Drug Details

Active Ingredients

IngredientStrength
GALLIC ACID MONOHYDRATE2 [hp_X]/1

OpenFDA Data

SPL SET ID:235eb705-8110-4b4f-822f-e2cf68780cfe
Manufacturer
UNII

NDC Crossover Matching brand name "GALLICUM ACIDUM" or generic name "Gallicum Acidum"

NDCBrand NameGeneric Name
0220-2231Gallicum acidumGALLIC ACID MONOHYDRATE
15631-0201GALLICUM ACIDUMGALLICUM ACIDUM
71919-308Gallicum acidumGALLIC ACID MONOHYDRATE
43742-0156Gallic AcidGallicum acidum
43742-0835Gallic AcidGallicum Acidum
43857-0234Gallic AcidGallicum Acidum

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