DRMITSUI ECZEMA RELIEF
- Product NDC
- 85248-181
- 11-digit product format
- 852480181
- Labeler code
- 85248
- Product ID
- 85248-181_4eee7637-3a29-e0bd-e063-6294a90ae1a4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Hydrocortisone 1% ECZEMA RELIEF
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Jiangxi Yudexi Pharmaceutical Co., LTD
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-04-08
- Substance
- HYDROCORTISONE
- Active strength
- 1 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- DRMITSUI ECZEMA RELIEF
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HYDROCORTISONE | 1 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | WI4X0X7BPJ |
| Rxcui | 106258 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85248-181-01 | DRMITSUI ECZEMA RELIEF | 20 g in 1 TUBE | CREAM | 20 | | 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 |
|---|
| 85248-181-01 | 85248018101 | 20 g in 1 TUBE (85248-181-01) | 20 g | 2026-04-08 | No | No | Current |