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