Aralia Racemosa MT

ARALIA RACEMOSA ORAL HUMAN PRESCRIPTION DRUG

Aralia Racemosa MT is an FDA drug label for the active ingredient ARALIA RACEMOSA manufactured by OHM PHARMA INC. administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20211228.

Generic name
ARALIA RACEMOSA
Manufacturer
OHM PHARMA INC.
Product type
HUMAN PRESCRIPTION DRUG
Route
ORAL
Dosage form
N/A
NDC
66096-751
Application
N/A
Label effective
20211228

Active ingredients

Active Ingredient: Aralia Racemosa MT

Indications & Usage

Batch no. 40021 Restest Date: 11/2022

Dosage & Administration

Not available.

Contraindications

Not available.

Warnings

Caution: for manufacturing,processing or repacking only. Caution: for manufacturing, processing or repacking only.

Adverse Reactions

Not available.

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ARALIA RACEMOSA

Aralia Racemosa

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