NDC 15631-0104

CANTHARIDINUM

Cantharidinum

CANTHARIDINUM 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 Cantharidin.

Product ID15631-0104_9ee8f0ea-e407-567e-e053-2a95a90ae7d8
NDC15631-0104
Product TypeHuman Otc Drug
Proprietary NameCANTHARIDINUM
Generic NameCantharidinum
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-06
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameCANTHARIDIN
Active Ingredient Strength8 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0104-0

100 PELLET in 1 PACKAGE (15631-0104-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0104-2 [15631010402]

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

NDC 15631-0104-0 [15631010400]

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

NDC 15631-0104-5 [15631010405]

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

NDC 15631-0104-4 [15631010404]

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

NDC 15631-0104-1 [15631010401]

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

NDC 15631-0104-3 [15631010403]

CANTHARIDINUM 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
CANTHARIDIN8 [hp_X]/1

OpenFDA Data

SPL SET ID:85b6b393-9795-40f7-87ff-96b5f3268d36
Manufacturer
UNII

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