Sedalia - 0220-9332-04 - (ACONITUM NAPELLUS, BELLADONNA LEAF, CALENDULA OFFICINALIS FLOWERING TOP, CHELIDONIUM MAJUS, ABRUS PRECATORIUS SEED, VIBURNUM OPULUS ROOT)

Alphabetical Index


Drug Information of Sedalia

Product NDC: 0220-9332
Proprietary Name: Sedalia
Non Proprietary Name: ACONITUM NAPELLUS, BELLADONNA LEAF, CALENDULA OFFICINALIS FLOWERING TOP, CHELIDONIUM MAJUS, ABRUS PRECATORIUS SEED, VIBURNUM OPULUS ROOT
Active Ingredient(s): 6; 6; 6; 6; 6; 6    [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1 & nbsp;   ACONITUM NAPELLUS, BELLADONNA LEAF, CALENDULA OFFICINALIS FLOWERING TOP, CHELIDONIUM MAJUS, ABRUS PRECATORIUS SEED, VIBURNUM OPULUS ROOT
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Sedalia

Product NDC: 0220-9332
Labeler Name: Laboratoires Boiron
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19970705

Package Information of Sedalia

Package NDC: 0220-9332-04
Package Description: 60 TABLET in 1 BLISTER PACK (0220-9332-04)

NDC Information of Sedalia

NDC Code 0220-9332-04
Proprietary Name Sedalia
Package Description 60 TABLET in 1 BLISTER PACK (0220-9332-04)
Product NDC 0220-9332
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ACONITUM NAPELLUS, BELLADONNA LEAF, CALENDULA OFFICINALIS FLOWERING TOP, CHELIDONIUM MAJUS, ABRUS PRECATORIUS SEED, VIBURNUM OPULUS ROOT
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970705
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Laboratoires Boiron
Substance Name ABRUS PRECATORIUS SEED; ACONITUM NAPELLUS; BELLADONNA LEAF; CALENDULA OFFICINALIS FLOWERING TOP; CHELIDONIUM MAJUS; VIBURNUM OPULUS ROOT
Strength Number 6; 6; 6; 6; 6; 6
Strength Unit [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1
Pharmaceutical Classes

Complete Information of Sedalia


General Information