NDC 15631-0009

AETHUSA CYNAPIUM

Aethusa Cynapium

AETHUSA CYNAPIUM 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 Aethusa Cynapium.

Product ID15631-0009_9e360e2b-b868-07c6-e053-2a95a90a4141
NDC15631-0009
Product TypeHuman Otc Drug
Proprietary NameAETHUSA CYNAPIUM
Generic NameAethusa Cynapium
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 NameAETHUSA CYNAPIUM
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0009-0

100 PELLET in 1 PACKAGE (15631-0009-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0009-2 [15631000902]

AETHUSA CYNAPIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0009-1 [15631000901]

AETHUSA CYNAPIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0009-3 [15631000903]

AETHUSA CYNAPIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0009-5 [15631000905]

AETHUSA CYNAPIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0009-0 [15631000900]

AETHUSA CYNAPIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

NDC 15631-0009-4 [15631000904]

AETHUSA CYNAPIUM PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-02-10

Drug Details

Active Ingredients

IngredientStrength
AETHUSA CYNAPIUM3 [hp_X]/1

OpenFDA Data

SPL SET ID:4147aa0d-7fee-468b-bb50-ae6d6fe729bc
Manufacturer
UNII

NDC Crossover Matching brand name "AETHUSA CYNAPIUM" or generic name "Aethusa Cynapium"

NDCBrand NameGeneric Name
0220-0104Aethusa cynapiumAETHUSA CYNAPIUM
0220-0105Aethusa cynapiumAETHUSA CYNAPIUM
0220-0109Aethusa cynapiumAETHUSA CYNAPIUM
15631-0009AETHUSA CYNAPIUMAETHUSA CYNAPIUM
60512-6450AETHUSA CYNAPIUMAETHUSA CYNAPIUM
62106-7220AETHUSA CYNAPIUMFools parsley
63545-067Aethusa cynapiumAethusa cynapium
63545-761Aethusa cynapiumAethusa cynapium
63545-762Aethusa cynapiumAethusa cynapium
63545-763Aethusa cynapiumAethusa cynapium
63545-764Aethusa cynapiumAethusa cynapium
63545-765Aethusa cynapiumAethusa cynapium
63545-766Aethusa cynapiumAethusa cynapium
66096-780Aethusa CynapiumAETHUSA CYNAPIUM
68428-183Aethusa CynapiumAethusa Cynapium
71919-018Aethusa cynapiumAethusa cynapium
64117-102Vomiting DiarrheaAETHUSA CYNAPIUM

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