Urevia 10
- Product NDC
- 85622-600
- 11-digit product format
- 856220600
- Labeler code
- 85622
- Product ID
- 85622-600_d4676f78-7141-49de-8c12-57a3b930090c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Urevia 10
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Blue Heron Pharmaceuticals, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2026-10-21
- Substance
- UREA
- Active strength
- 100 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Urevia 10
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| UREA | 100 mg/mL |