Spongilla lacustris MT
Spongilla lacustris MT is an FDA drug label for the active ingredient SPONGILLA LACUSTRIS 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 20211229.
Generic: SPONGILLA LACUSTRIS
Manufacturer: OHM PHARMA INC.
Product Type: HUMAN PRESCRIPTION DRUG
Route: ORAL
Dosage Form:
NDC: 66096-749
Application:
Effective: 20211229
Active Ingredients: Active Ingredient: Spongilla Lacustris
Indications & Usage
Not available.
Dosage & Administration
Not available.
Contraindications
Not available.
Warnings
Caution: for manufacturing, processing or repacking only.
Adverse Reactions
Not available.