NDC 69968-0835-01 - Neutrogena SkinClearing Mineral Powder Honey 85
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
- 69968-0835
- Requested NDC
- 69968-0835-01
- Package NDCs from labels
- 69968-0835-1, 69968-0835-01
- Manufacturer
- Kenvue Brands LLC
- Effective date
- 2024-11-13
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Neutrogena SkinClearing Mineral Powder Honey 85 - Kenvue Brands LLC | Kenvue Brands LLC | 2024-11-13 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69968-0835-1 | Neutrogena SkinClearing Mineral Powder Natural Beige 60 | 11 g in 1 CONTAINER | POWDER | 11 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 69968-0835 | NEUTROGENA SKINCLEARING MINERAL POWDER HONEY 85 (SALICYLIC ACID) POWDER NEUTROGENA SKINCLEARING MINERAL POWDER CHESTNUT 135 (SALICYLIC ACID) POWDER NEUTROGENA SKINCLEARING MINERAL POWDER NATURAL BEIGE 60 (SALICYLIC ACID) POWDER NEUTROGENA SKINCLEARING MINERAL POWDER SOFT BEIGE 50 (SALICYLIC ACID) POWDER NEUTROGENA SKINCLEARING MINERAL POWDER NATURAL IVORY 20 (SALICYLIC ACID) POWDER NEUTROGENA SKINCLEARING MINERAL POWDER BUFF 30 (SALICYLIC ACID) POWDER NEUTROGENA SKINCLEARING MINERAL POWDER CLASSIC IVORY 10 (SALICYLIC ACID) POWDER NEUTROGENA SKINCLEARING MINERAL POWDER NUDE 40 (SALICYLIC ACID) POWDER [KENVUE BRANDS LLC] | 2 | Current NDC, 1 package rows | 20241115_0d1556d3-d689-c4c1-e063-6394a90adab0.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.