Camilia - 0220-9054-09 - (MATRICARIA RECUTITA, RHUBARB, PHYTOLACCA AMERICANA ROOT)

Alphabetical Index


Drug Information of Camilia

Product NDC: 0220-9054
Proprietary Name: Camilia
Non Proprietary Name: MATRICARIA RECUTITA, RHUBARB, PHYTOLACCA AMERICANA ROOT
Active Ingredient(s): 9; 5; 5    [hp_C]/1; [hp_C]/1; [hp_C]/1 & nbsp;   MATRICARIA RECUTITA, RHUBARB, PHYTOLACCA AMERICANA ROOT
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Camilia

Product NDC: 0220-9054
Labeler Name: Laboratoires Boiron
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20101201

Package Information of Camilia

Package NDC: 0220-9054-09
Package Description: 30 LIQUID in 1 BOX (0220-9054-09)

NDC Information of Camilia

NDC Code 0220-9054-09
Proprietary Name Camilia
Package Description 30 LIQUID in 1 BOX (0220-9054-09)
Product NDC 0220-9054
Product Type Name HUMAN OTC DRUG
Non Proprietary Name MATRICARIA RECUTITA, RHUBARB, PHYTOLACCA AMERICANA ROOT
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20101201
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Laboratoires Boiron
Substance Name MATRICARIA RECUTITA; PHYTOLACCA AMERICANA ROOT; RHUBARB
Strength Number 9; 5; 5
Strength Unit [hp_C]/1; [hp_C]/1; [hp_C]/1
Pharmaceutical Classes

Complete Information of Camilia


General Information