Product NDC: | 58666-3122 |
Proprietary Name: | Eczema and Psoriasis Therapy |
Non Proprietary Name: | FUCUS VESICULOSUS, CENTELLA ASIATICA, MELISSA OFFICINALIS, ALOE |
Active Ingredient(s): | 1; 1; 1; 1 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g & nbsp; FUCUS VESICULOSUS, CENTELLA ASIATICA, MELISSA OFFICINALIS, ALOE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOAP |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 58666-3122 |
Labeler Name: | Sundial Group LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20130601 |
Package NDC: | 58666-3122-6 |
Package Description: | 141 g in 1 PACKAGE (58666-3122-6) |
NDC Code | 58666-3122-6 |
Proprietary Name | Eczema and Psoriasis Therapy |
Package Description | 141 g in 1 PACKAGE (58666-3122-6) |
Product NDC | 58666-3122 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | FUCUS VESICULOSUS, CENTELLA ASIATICA, MELISSA OFFICINALIS, ALOE |
Dosage Form Name | SOAP |
Route Name | TOPICAL |
Start Marketing Date | 20130601 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Sundial Group LLC |
Substance Name | ALOE; CENTELLA ASIATICA; FUCUS VESICULOSUS; MELISSA OFFICINALIS |
Strength Number | 1; 1; 1; 1 |
Strength Unit | [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g |
Pharmaceutical Classes |