Hydroryx
- Product NDC
- 85477-317
- 11-digit product format
- 854770317
- Labeler code
- 85477
- Product ID
- 85477-317_99c16242-0a08-4a87-b23d-f773a444a18d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocortisone 2%
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Oncora Pharma, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2025-10-22
- Substance
- HYDROCORTISONE
- Active strength
- 2 g/100g
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- 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
- Hydroryx
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HYDROCORTISONE | 2 g/100g |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85477-317-28 | 85477031728 | 28 g in 1 TUBE (85477-317-28) | 28 g | 2025-10-22 | No | No | Current |