Drugplain

PASSIFLORA PLEX 10 [hp_X]/30mL

Passiflora incarnata, Ignatia amara, Jalapa, Coffea cruda, Magnesium metalicum, Palladium metallicum, Tellurium metallicum, Phosphoricum acidum · LIQUID · SanUp

No Recall History
Plain English

Passiflora Plex is an over-the-counter sublingual liquid containing a combination of herbal and mineral ingredients used to support relaxation and calm. This product is classified as a non-standardized food allergenic extract and should not be used by individuals with allergies to any of its components.

Key Facts

Brand Name
PASSIFLORA PLEX
Generic Name
Passiflora incarnata, Ignatia amara, Jalapa, Coffea cruda, Magnesium metalicum, Palladium metallicum, Tellurium metallicum, Phosphoricum acidum
NDC Code (Product)
52503-1322
Manufacturer
SanUp
Strength
10 [hp_X]/30mL
Dosage Form
LIQUID
Route
SUBLINGUAL
Marketing Status
Drug Class
Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]
Marketing Start
02/09/2015

Recall History

No Recall History

Frequently Asked Questions

What is PASSIFLORA PLEX used for?

Passiflora Plex is an over-the-counter sublingual liquid containing a combination of herbal and mineral ingredients used to support relaxation and calm. This product is classified as a non-standardized food allergenic extract and should not be used by individuals with allergies to any of its components.

Is PASSIFLORA PLEX a controlled substance?

PASSIFLORA PLEX is not classified as a controlled substance by the DEA.

What is the generic name for PASSIFLORA PLEX?

The generic name for PASSIFLORA PLEX is Passiflora incarnata, Ignatia amara, Jalapa, Coffea cruda, Magnesium metalicum, Palladium metallicum, Tellurium metallicum, Phosphoricum acidum. There are 1 other brand versions of Passiflora incarnata, Ignatia amara, Jalapa, Coffea cruda, Magnesium metalicum, Palladium metallicum, Tellurium metallicum, Phosphoricum acidum.

What is the NDC code for PASSIFLORA PLEX 10 [hp_X]/30mL?

The NDC (National Drug Code) for PASSIFLORA PLEX 10 [hp_X]/30mL is 52503-1322, listed by SanUp.

Product NDC

52503-1322

Package NDC

52503-1322-0

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

Data from openFDA · Public domain (CC0 1.0)