Drugplain

Aesculus 1 [hp_X]/mL

Potentilla Anserina, Aesculus Hippocastanum, Ustilago Maidis, Secale Cornutum, Ruta Graveolens · LIQUID · Marco Pharma International LLC.

No Recall History
Plain English

Aesculus is a liquid containing potentilla anserina, aesculus hippocastanum, ustilago maidis, secale cornutum, ruta graveolens at 1 [hp_X]/mL, taken oral. Manufactured by Marco Pharma International LLC..

Key Facts

Brand Name
Aesculus
Generic Name
Potentilla Anserina, Aesculus Hippocastanum, Ustilago Maidis, Secale Cornutum, Ruta Graveolens
NDC Code (Product)
60986-1027
Manufacturer
Marco Pharma International LLC.
Strength
1 [hp_X]/mL
Dosage Form
LIQUID
Route
ORAL
Marketing Status
Drug Class
Non-Standardized Fungal Allergenic Extract [EPC]
Marketing Start
03/01/1992

Recall History

No Recall History

Frequently Asked Questions

What is Aesculus used for?

Aesculus contains Potentilla Anserina, Aesculus Hippocastanum, Ustilago Maidis, Secale Cornutum, Ruta Graveolens. It is a liquid taken oral. Consult your doctor for specific uses.

Is Aesculus a controlled substance?

Aesculus is not classified as a controlled substance by the DEA.

What is the generic name for Aesculus?

The generic name for Aesculus is Potentilla Anserina, Aesculus Hippocastanum, Ustilago Maidis, Secale Cornutum, Ruta Graveolens. There are no other listed brand versions of Potentilla Anserina, Aesculus Hippocastanum, Ustilago Maidis, Secale Cornutum, Ruta Graveolens.

What is the NDC code for Aesculus 1 [hp_X]/mL?

The NDC (National Drug Code) for Aesculus 1 [hp_X]/mL is 60986-1027, listed by Marco Pharma International LLC..

Product NDC

60986-1027

Package NDC

60986-1027-3

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)