Aesculus - 60986-1027-3 - (Potentilla Anserina, Aesculus Hippocastanum, Ustilago Maidis, Secale Cornutum, Ruta Graveolens)

Alphabetical Index


Drug Information of Aesculus

Product NDC: 60986-1027
Proprietary Name: Aesculus
Non Proprietary Name: Potentilla Anserina, Aesculus Hippocastanum, Ustilago Maidis, Secale Cornutum, Ruta Graveolens
Active Ingredient(s): 1; 4; 1; 3; 5    [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp;   Potentilla Anserina, Aesculus Hippocastanum, Ustilago Maidis, Secale Cornutum, Ruta Graveolens
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Aesculus

Product NDC: 60986-1027
Labeler Name: Marco Pharma International LLC.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 19920301

Package Information of Aesculus

Package NDC: 60986-1027-3
Package Description: 50 mL in 1 BOTTLE, GLASS (60986-1027-3)

NDC Information of Aesculus

NDC Code 60986-1027-3
Proprietary Name Aesculus
Package Description 50 mL in 1 BOTTLE, GLASS (60986-1027-3)
Product NDC 60986-1027
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Potentilla Anserina, Aesculus Hippocastanum, Ustilago Maidis, Secale Cornutum, Ruta Graveolens
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 19920301
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Marco Pharma International LLC.
Substance Name ARGENTINA ANSERINA FLOWERING TOP; CLAVICEPS PURPUREA SCLEROTIUM; HORSE CHESTNUT; RUTA GRAVEOLENS WHOLE; USTILAGO MAYDIS
Strength Number 1; 4; 1; 3; 5
Strength Unit [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmaceutical Classes

Complete Information of Aesculus


General Information