ADAPALENE AND BENZOYL PEROXIDE
- Product NDC
- 72162-1432
- 11-digit product format
- 721621432
- Labeler code
- 72162
- Product ID
- 72162-1432_34d97051-0ad6-442e-8424-252f2ebac5e3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- adapalene and benzoyl peroxide
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA212464
- Marketing category
- ANDA
- Marketing start
- 2022-06-02
- Substance
- ADAPALENE; BENZOYL PEROXIDE
- Active strength
- 3; 25 mg/g; mg/g
- Pharmacologic classes
- Retinoid [EPC], Retinoids [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 1L4806J2QF | ADAPALENE | 106685-40-9 | ADAPALENE |
| W9WZN9A0GM | BENZOYL PEROXIDE | 94-36-0 | BENZOYL PEROXIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1432-2 | 72162143202 | 45 g in 1 BOTTLE, PUMP (72162-1432-2) | 45 g | 2024-03-13 | No | No | Historical |