NDC 64942-2003-01 - Dove
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
- 64942-2003
- Requested NDC
- 64942-2003-01
- Package NDCs from labels
- 64942-2003-1, 64942-2003-01
- Manufacturer
- Conopco, Inc. d/b/a Unilever
- Effective date
- 2024-11-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Dove - Conopco, Inc. d/b/a Unilever | Conopco, Inc. d/b/a Unilever | 2024-11-06 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 64942-2003-1 | Dove | 107 g in 1 CAN | AEROSOL, SPRAY | 107 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 64942-2003 | DOVE (ADVANCED CARE DRY SPRAY PASSION FRUIT AND LEMONGRASS 48H ANTIPERSPIRANT DEODORANT) AEROSOL, SPRAY [CONOPCO, INC. D/B/A UNILEVER] | 2 | Current NDC, Legacy NDC, 1 package rows | 20241108_d9a555fe-2c89-05e6-e053-2a95a90aba56.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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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.