NDC 15631-0318

OENANTHE CROCATA

Oenanthe Crocata

OENANTHE CROCATA 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 Oenanthe Crocata Root.

Product ID15631-0318_a199c8a3-0b48-4a79-e053-2995a90a9d2f
NDC15631-0318
Product TypeHuman Otc Drug
Proprietary NameOENANTHE CROCATA
Generic NameOenanthe Crocata
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 NameOENANTHE CROCATA ROOT
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0318-0

100 PELLET in 1 PACKAGE (15631-0318-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0318-5 [15631031805]

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

NDC 15631-0318-3 [15631031803]

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

NDC 15631-0318-1 [15631031801]

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

NDC 15631-0318-2 [15631031802]

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

NDC 15631-0318-0 [15631031800]

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

NDC 15631-0318-4 [15631031804]

OENANTHE CROCATA 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
OENANTHE CROCATA ROOT3 [hp_X]/1

OpenFDA Data

SPL SET ID:4d01e413-d256-4010-af04-f0c2dab34052
Manufacturer
UNII

NDC Crossover Matching brand name "OENANTHE CROCATA" or generic name "Oenanthe Crocata"

NDCBrand NameGeneric Name
0220-3752Oenanthe crocataOENANTHE CROCATA ROOT
15631-0318OENANTHE CROCATAOENANTHE CROCATA
63545-664Oenanthe CrocataOenanthe Crocata
71919-501OENANTHEOenanthe crocata

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