NDC 69968-0761-01 - Neutrogena Stubborn Acne Spot Drying
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
- 69968-0761
- Requested NDC
- 69968-0761-01
- Package NDCs from labels
- 69968-0761-1, 69968-0761-01
- Manufacturer
- Kenvue Brands LLC
- Effective date
- 2024-11-26
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Neutrogena Stubborn Acne Spot Drying - Kenvue Brands LLC | Kenvue Brands LLC | 2024-11-26 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69968-0761-1 | Neutrogena Stubborn Acne Spot Drying | 29 mL in 1 BOTTLE | LOTION | 29 | 4 | |
| 69968-0761-1 | Neutrogena Stubborn Acne Spot Drying | 1 in 1 CARTON | LOTION | 1 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 69968-0761 | NEUTROGENA STUBBORN ACNE SPOT DRYING (SULFUR) LOTION [KENVUE BRANDS LLC] | 4 | Current NDC, Legacy NDC, 2 package rows | 20241208_dffe9bf4-a8a2-4fa0-e053-2995a90abcb3.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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.