NDC 15631-0118

CAUSTICUM

Causticum

CAUSTICUM 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 Causticum.

Product ID15631-0118_0a04317f-30e5-4557-b76c-def11140784f
NDC15631-0118
Product TypeHuman Otc Drug
Proprietary NameCAUSTICUM
Generic NameCausticum
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 NameCAUSTICUM
Active Ingredient Strength2 [hp_X]/1
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 15631-0118-0

100 PELLET in 1 PACKAGE (15631-0118-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0118-5 [15631011805]

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

NDC 15631-0118-2 [15631011802]

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

NDC 15631-0118-4 [15631011804]

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

NDC 15631-0118-3 [15631011803]

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

NDC 15631-0118-1 [15631011801]

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

NDC 15631-0118-0 [15631011800]

CAUSTICUM 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
CAUSTICUM2 [hp_X]/1

OpenFDA Data

SPL SET ID:9951fbb9-6a8e-45c8-bf82-5889dfd2148f
Manufacturer
UNII

NDC Crossover Matching brand name "CAUSTICUM" or generic name "Causticum"

NDCBrand NameGeneric Name
0220-1216CausticumCAUSTICUM
0220-1217CausticumCAUSTICUM
0220-1220CausticumCAUSTICUM
0220-1224CausticumCAUSTICUM
0220-1227CausticumCAUSTICUM
0220-1229CausticumCAUSTICUM
0220-1233CausticumCAUSTICUM
0220-1236CausticumCAUSTICUM
0220-1237CausticumCAUSTICUM
0220-1240CausticumCAUSTICUM
0220-1241CausticumCAUSTICUM
0360-0114CAUSTICUMCAUSTICUM
0360-0115CAUSTICUMCAUSTICUM
15631-0118CAUSTICUMCAUSTICUM
15631-0556CAUSTICUMCAUSTICUM
44911-0384CausticumCausticum
60512-6228CAUSTICUMCAUSTICUM
62106-4986CAUSTICUMHahnemanns causticum
63083-7113CausticumCausticum
66096-813CausticumCAUSTICUM
68428-295CausticumCAUSTICUM
71919-171CausticumCAUSTICUM
76472-4040CAUSTICUMCAUSTICUM
76472-4072CAUSTICUMCAUSTICUM
43406-0306Causticum 200CCausticum
68428-041Causticum Kit RefillCAUSTICUM
68428-091Causticum Kit RefillCAUSTICUM

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