Product NDC: | 10191-2034 |
Proprietary Name: | LYCOPODIUM CLAVATUM |
Non Proprietary Name: | CLUBMOSS |
Active Ingredient(s): | 9 [hp_C]/1 & nbsp; CLUBMOSS |
Administration Route(s): | SUBLINGUAL |
Dosage Form(s): | PELLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10191-2034 |
Labeler Name: | REMEDY MAKERS |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20030507 |
Package NDC: | 10191-2034-2 |
Package Description: | 138 PELLET in 1 VIAL, GLASS (10191-2034-2) |
NDC Code | 10191-2034-2 |
Proprietary Name | LYCOPODIUM CLAVATUM |
Package Description | 138 PELLET in 1 VIAL, GLASS (10191-2034-2) |
Product NDC | 10191-2034 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | CLUBMOSS |
Dosage Form Name | PELLET |
Route Name | SUBLINGUAL |
Start Marketing Date | 20030507 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | REMEDY MAKERS |
Substance Name | LYCOPODIUM CLAVATUM SPORE |
Strength Number | 9 |
Strength Unit | [hp_C]/1 |
Pharmaceutical Classes |