NDC 15631-0198

FRAXINUS AMERICANA

Fraxinus Americana

FRAXINUS AMERICANA 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 Fraxinus Americana Bark.

Product ID15631-0198_00582ce0-43e4-4bfb-8664-ca8cb9ec3b52
NDC15631-0198
Product TypeHuman Otc Drug
Proprietary NameFRAXINUS AMERICANA
Generic NameFraxinus Americana
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-25
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameFRAXINUS AMERICANA BARK
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0198-0

100 PELLET in 1 PACKAGE (15631-0198-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0198-2 [15631019802]

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

NDC 15631-0198-3 [15631019803]

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

NDC 15631-0198-1 [15631019801]

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

NDC 15631-0198-5 [15631019805]

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

NDC 15631-0198-4 [15631019804]

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

NDC 15631-0198-0 [15631019800]

FRAXINUS AMERICANA 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
FRAXINUS AMERICANA BARK1 [hp_X]/1

OpenFDA Data

SPL SET ID:73e4c131-66f7-48e7-9063-803a1248c85f
Manufacturer
UNII

NDC Crossover Matching brand name "FRAXINUS AMERICANA" or generic name "Fraxinus Americana"

NDCBrand NameGeneric Name
0220-2155Fraxinus americanaFRAXINUS AMERICANA BARK
0220-2156Fraxinus americanaFRAXINUS AMERICANA BARK
15631-0198FRAXINUS AMERICANAFRAXINUS AMERICANA
15631-0586FRAXINUS AMERICANAFRAXINUS AMERICANA
68428-394Fraxinus americanaFRAXINUS AMERICANA BARK
71919-303Fraxinus americanaFRAXINUS AMERICANA BARK
22840-1425White Ash PollenFraxinus americana
22840-1426White Ash PollenFraxinus americana
22840-1427White Ash PollenFraxinus americana
22840-1428White Ash PollenFraxinus americana
22840-4430White Ash PollenFraxinus americana
22840-5407White Ash PollenFraxinus americana
49643-357White Ash PollenFraxinus americana

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