# Dermoyrx

NDC: 85477-910
Generic name: Urea 41%
Labeler / Manufacturer: Oncora Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Unapproved drug (not FDA-reviewed)
Dosage form: CREAM
Routes: TOPICAL
Marketing started: 20261028



## Active ingredients

- UREA: 410 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"85477-910"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=85477-910