Hydrocortisone Acetate Pramoxine Hcl
- Product NDC
- 71335-2942
- 11-digit product format
- 713352942
- Labeler code
- 71335
- Product ID
- 71335-2942_1cb486db-e980-4ebe-83a1-d8c2b5cdce37
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hydrocortisone Acetate Pramoxine Hcl
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 1996-09-27
- Substance
- HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE
- Active strength
- 2.5; 1 g/100g; g/100g
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 3X7931PO74 | HYDROCORTISONE ACETATE | 50-03-3 | HYDROCORTISONE ACETATE |
| 88AYB867L5 | PRAMOXINE HYDROCHLORIDE | 637-58-1 | PRAMOXINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2942-1 | 71335294201 | 30 TUBE in 1 CARTON (71335-2942-1) / 4 g in 1 TUBE | 30 tube | 2025-10-28 | No | No | Historical |