CHAMOMILLA - 10191-1361-2 - (CHAMOMILE PLANT)

Alphabetical Index


Drug Information of CHAMOMILLA

Product NDC: 10191-1361
Proprietary Name: CHAMOMILLA
Non Proprietary Name: CHAMOMILE PLANT
Active Ingredient(s): 6    [hp_C]/1 & nbsp;   CHAMOMILE PLANT
Administration Route(s): SUBLINGUAL
Dosage Form(s): PELLET
Coding System: National Drug Codes(NDC)

Labeler Information of CHAMOMILLA

Product NDC: 10191-1361
Labeler Name: Remedy Makers
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20041015

Package Information of CHAMOMILLA

Package NDC: 10191-1361-2
Package Description: 155 PELLET in 1 VIAL, GLASS (10191-1361-2)

NDC Information of CHAMOMILLA

NDC Code 10191-1361-2
Proprietary Name CHAMOMILLA
Package Description 155 PELLET in 1 VIAL, GLASS (10191-1361-2)
Product NDC 10191-1361
Product Type Name HUMAN OTC DRUG
Non Proprietary Name CHAMOMILE PLANT
Dosage Form Name PELLET
Route Name SUBLINGUAL
Start Marketing Date 20041015
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Remedy Makers
Substance Name MATRICARIA RECUTITA
Strength Number 6
Strength Unit [hp_C]/1
Pharmaceutical Classes

Complete Information of CHAMOMILLA


General Information