Product NDC: | 48951-7029 |
Proprietary Name: | Melissa Chamomilla Menopause Relief |
Non Proprietary Name: | MATRICARIA RECUTITA MELISSA OFFICINALIS ACONITUM NAPELLUS ROOT LACHESIS MUTA VENOM |
Active Ingredient(s): | 10; 12; 3; 3 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp; MATRICARIA RECUTITA MELISSA OFFICINALIS ACONITUM NAPELLUS ROOT LACHESIS MUTA VENOM |
Administration Route(s): | ORAL |
Dosage Form(s): | PELLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 48951-7029 |
Labeler Name: | Uriel Pharmacy Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20090901 |
Package NDC: | 48951-7029-2 |
Package Description: | 1350 PELLET in 1 BOTTLE, GLASS (48951-7029-2) |
NDC Code | 48951-7029-2 |
Proprietary Name | Melissa Chamomilla Menopause Relief |
Package Description | 1350 PELLET in 1 BOTTLE, GLASS (48951-7029-2) |
Product NDC | 48951-7029 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | MATRICARIA RECUTITA MELISSA OFFICINALIS ACONITUM NAPELLUS ROOT LACHESIS MUTA VENOM |
Dosage Form Name | PELLET |
Route Name | ORAL |
Start Marketing Date | 20090901 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Uriel Pharmacy Inc |
Substance Name | ACONITUM NAPELLUS ROOT; LACHESIS MUTA VENOM; MATRICARIA RECUTITA; MELISSA OFFICINALIS |
Strength Number | 10; 12; 3; 3 |
Strength Unit | [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 |
Pharmaceutical Classes |