Oxy Maximum Strength Rapid Spot Treatment
- Product NDC
- 10742-1002
- 11-digit product format
- 107421002
- Labeler code
- 10742
- Product ID
- 10742-1002_28886273-a71b-46ea-e063-6394a90ac11d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Oxy Maximum Strength Rapid Spot Treatment
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- The Mentholatum Company
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-08-15
- Substance
- BENZOYL PEROXIDE
- Active strength
- 100 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| W9WZN9A0GM | BENZOYL PEROXIDE | 94-36-0 | BENZOYL PEROXIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 10742-1002-1 | 10742100201 | 1 TUBE in 1 CARTON (10742-1002-1) / 28 g in 1 TUBE | 1 tube | 2024-08-15 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Drug Facts | The Mentholatum Company | 2024-12-05 | HUMAN OTC DRUG LABEL | 1 |