NDC 69968-0256-01 - Neutrogena Revitalizing Lip Balm SPF 20 - Fresh Plum 60
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
- 69968-0256
- Requested NDC
- 69968-0256-01
- Package NDCs from labels
- 69968-0256-1, 69968-0256-01
- Manufacturer
- Kenvue Brands LLC
- Effective date
- 2024-11-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Neutrogena Revitalizing Lip Balm SPF 20 - Fresh Plum 60 - Kenvue Brands LLC | Kenvue Brands LLC | 2024-11-11 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69968-0256-1 | Neutrogena Revitalizing Lip BalmSPF 20 - Fresh Plum 60 | 1 in 1 BLISTER PACK | LIPSTICK | 1 | 7 | |
| 69968-0256-1 | Neutrogena Revitalizing Lip BalmSPF 20 - Fresh Plum 60 | 4.2 g in 1 TUBE | LIPSTICK | 4.2 | 7 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 69968-0256 | NEUTROGENA REVITALIZING LIP BALM SPF 20 - FRESH PLUM 60 (OCTINOXATE AND OXYBENZONE) LIPSTICK NEUTROGENA REVITALIZING LIP BALM SPF 20 - SHEEER SHIMMER 10 (OCTINOXATE AND OXYBENZONE) LIPSTICK NEUTROGENA REVITALIZING LIP BALM SPF 20 - SOFT CARAMEL 50 (OCTINOXATE AND OXYBENZONE) LIPSTICK NEUTROGENA REVITALIZING LIP BALM SPF 20 - HEALTHY BLUSH 20 (OCTINOXATE AND OXYBENZONE) LIPSTICK NEUTROGENA REVITALIZING LIP BALM SPF 20 - SUNNY BERRY 30 (OCTINOXATE AND OXYBENZONE) LIPSTICK NEUTROGENA REVITALIZING LIP BALM SPF 20 - PETAL GLOW 40 (OCTINOXATE AND OXYBENZONE) LIPSTICK [KENVUE BRANDS LLC] | 7 | Current NDC, Legacy NDC, 2 package rows | 20241114_e77c07d4-4e64-4000-9e7a-963aa6c6448c.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.