# Urea 39

NDC: 87021-602
Generic name: Urea
Labeler / Manufacturer: Krewe Pharma, LLC
Product type: HUMAN OTC DRUG
Marketing category: Unapproved drug (not FDA-reviewed)
Dosage form: CREAM
Routes: TOPICAL
Marketing started: 20260602



## Active ingredients

- UREA: 390 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"87021-602"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=87021-602
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=be19358f-67a8-4a0d-88e0-91eb4cb42e0d