Product NDC: | 51393-5622 |
Proprietary Name: | Eczema Control |
Non Proprietary Name: | Centella Asiatica, Iris Versicolor Root, Arctium Lappa Root, Sodium Chloride, Ruta Graveolens Flowering Top, Silicon Dioxide, Taraxacum Officinale, and Thuja Occidentalis Root |
Active Ingredient(s): | 12; 12; 12; 12; 6; 12; 6; 8 [hp_C]/100mL; [hp_C]/100mL; [hp_C]/100mL; [hp_C]/100mL; [hp_X]/1000mL; [hp_X]/1000mL; [hp_C]/100mL; [hp_X]/1000mL & nbsp; Centella Asiatica, Iris Versicolor Root, Arctium Lappa Root, Sodium Chloride, Ruta Graveolens Flowering Top, Silicon Dioxide, Taraxacum Officinale, and Thuja Occidentalis Root |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51393-5622 |
Labeler Name: | Forces of Nature |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20111201 |
Package NDC: | 51393-5622-2 |
Package Description: | 33 mL in 1 BOTTLE, DISPENSING (51393-5622-2) |
NDC Code | 51393-5622-2 |
Proprietary Name | Eczema Control |
Package Description | 33 mL in 1 BOTTLE, DISPENSING (51393-5622-2) |
Product NDC | 51393-5622 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Centella Asiatica, Iris Versicolor Root, Arctium Lappa Root, Sodium Chloride, Ruta Graveolens Flowering Top, Silicon Dioxide, Taraxacum Officinale, and Thuja Occidentalis Root |
Dosage Form Name | SOLUTION/ DROPS |
Route Name | TOPICAL |
Start Marketing Date | 20111201 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Forces of Nature |
Substance Name | ARCTIUM LAPPA ROOT; CENTELLA ASIATICA; IRIS VERSICOLOR ROOT; RUTA GRAVEOLENS FLOWERING TOP; SILICON DIOXIDE; SODIUM CHLORIDE; TARAXACUM OFFICINALE; THUJA OCCIDENTALIS ROOT |
Strength Number | 12; 12; 12; 12; 6; 12; 6; 8 |
Strength Unit | [hp_C]/100mL; [hp_C]/100mL; [hp_C]/100mL; [hp_C]/100mL; [hp_X]/1000mL; [hp_X]/1000mL; [hp_C]/100mL; [hp_X]/1000mL |
Pharmaceutical Classes |