Hydrocortisone
- Product NDC
- 71741-455
- 11-digit product format
- 717410455
- Labeler code
- 71741
- Product ID
- 71741-455_c5cf0d24-3d06-4062-a10d-b3203486954f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydrocortisone
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Redmont Pharmaceuticals, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2026-03-24
- Substance
- HYDROCORTISONE
- Active strength
- 20 mg/g
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Hydrocortisone
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HYDROCORTISONE | 20 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | WI4X0X7BPJ |
| Rxcui | 604449 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71741-455-31 | Hydrocortisone | 30 g in 1 TUBE | GEL | 30 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71741-455-31 | 71741045531 | 30 g in 1 TUBE (71741-455-31) | 30 g | 2026-03-24 | No | No | Historical |