NDC 15631-0119

CEANOTHUS AMERICANUS

Ceanothus Americanus

CEANOTHUS AMERICANUS 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 Ceanothus Americanus Leaf.

Product ID15631-0119_9ee9a098-d31f-b396-e053-2995a90a8e77
NDC15631-0119
Product TypeHuman Otc Drug
Proprietary NameCEANOTHUS AMERICANUS
Generic NameCeanothus Americanus
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 NameCEANOTHUS AMERICANUS LEAF
Active Ingredient Strength1 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0119-0

100 PELLET in 1 PACKAGE (15631-0119-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0119-0 [15631011900]

CEANOTHUS AMERICANUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0119-1 [15631011901]

CEANOTHUS AMERICANUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0119-3 [15631011903]

CEANOTHUS AMERICANUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0119-5 [15631011905]

CEANOTHUS AMERICANUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0119-4 [15631011904]

CEANOTHUS AMERICANUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

NDC 15631-0119-2 [15631011902]

CEANOTHUS AMERICANUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-19

Drug Details

Active Ingredients

IngredientStrength
CEANOTHUS AMERICANUS LEAF1 [hp_X]/1

OpenFDA Data

SPL SET ID:fe50be77-1e6e-48c7-83e5-196f85e81313
Manufacturer
UNII

NDC Crossover Matching brand name "CEANOTHUS AMERICANUS" or generic name "Ceanothus Americanus"

NDCBrand NameGeneric Name
0220-1231Ceanothus americanusCEANOTHUS AMERICANUS LEAF
15631-0119CEANOTHUS AMERICANUSCEANOTHUS AMERICANUS
15631-0557CEANOTHUS AMERICANUSCEANOTHUS AMERICANUS
37662-0217Ceanothus AmericanusCeanothus Americanus
37662-0218Ceanothus AmericanusCeanothus Americanus
37662-0219Ceanothus AmericanusCeanothus Americanus
37662-0220Ceanothus AmericanusCeanothus Americanus
37662-0221Ceanothus AmericanusCeanothus Americanus
37662-0222Ceanothus AmericanusCeanothus Americanus
37662-0223Ceanothus AmericanusCeanothus Americanus
37662-0224Ceanothus AmericanusCeanothus Americanus
68428-296Ceanothus americanusCEANOTHUS AMERICANUS LEAF
71919-172Ceanothus americanusCEANOTHUS AMERICANUS LEAF

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