NDC 10742-1002-01 - Oxy Maximum Strength Rapid Spot Treatment
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 10742-1002
- Requested NDC
- 10742-1002-01
- Package NDCs from labels
- 10742-1002-1, 10742-1002-01
- Manufacturer
- The Mentholatum Company
- Effective date
- 2024-12-05
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Oxy Maximum Strength Rapid Spot Treatment - The Mentholatum Company | The Mentholatum Company | 2024-12-05 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 10742-1002-1 | Oxy Maximum Strength Rapid Spot Treatment | 1 in 1 CARTON | CREAM | 1 | 1 | |
| 10742-1002-1 | Oxy Maximum Strength Rapid Spot Treatment | 28 g in 1 TUBE | CREAM | 28 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 10742-1002 | OXY MAXIMUM STRENGTH RAPID SPOT TREATMENT CREAM [THE MENTHOLATUM COMPANY] | 1 | Current NDC, 2 package rows | 20241208_28886273-a71a-46ea-e063-6394a90ac11d.zip |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
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