ALUBRI
- Product NDC
- 87941-101
- 11-digit product format
- 879410101
- Labeler code
- 87941
- Product ID
- 87941-101_9cd4dfbb-2302-4bee-810b-09717c4d2e2d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Hydrocortisone
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Venus Health Science, Inc.
- Application
- m016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-08-18
- Substance
- HYDROCORTISONE
- Active strength
- 2.5 mg/mL
- 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
- ALUBRI
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HYDROCORTISONE | 2.5 mg/mL |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87941-101-20 | 87941010120 | 30 mL in 1 TUBE (87941-101-20) | 30 ml | 2026-08-18 | No | No | Current |