NDC 0135-0613 - AQUAFRESH whitening intense white
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
- 0135-0613
- Package NDCs from labels
- 0135-0613-01
- Manufacturer
- Haleon US Holdings LLC
- Effective date
- 2024-04-24
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| AQUAFRESH whitening intense white - Haleon US Holdings LLC | Haleon US Holdings LLC | 2024-04-24 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0135-0613-01 | AQUAFRESH whiteningwhite and shine | 121.9 g in 1 TUBE | PASTE | 121.9 | 4 | |
| 0135-0613-01 | AQUAFRESH whiteningwhite and shine | 1 in 1 CARTON | PASTE | 1 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 0135-0613 | AQUAFRESH WHITENING INTENSE WHITE (SODIUM FLUORIDE) PASTE AQUAFRESH WHITENING WHITE AND SHINE (SODIUM FLUORIDE) PASTE [HALEON US HOLDINGS LLC] | 4 | 2 package rows | 20240426_8baed730-f9a1-40ea-83fc-dcc6bd0ac62f.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.