NDC 64651-7749-01 - Intellishade Original SPF 45
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
- 64651-7749
- Requested NDC
- 64651-7749-01
- Package NDCs from labels
- 64651-7749-1, 64651-7749-2, 64651-7749-3, 64651-7749-01
- Manufacturer
- Revision, LLC | Goodier Cosmetics LP
- Effective date
- 2026-01-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Intellishade Original SPF 45 - Revision, LLC | Goodier Cosmetics LP | Revision, LLC | Goodier Cosmetics LP | 2026-01-12 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 64651-7749-1 | Intellishade Original SPF 45 | 48 g in 1 TUBE | CREAM | 48 | 13 | |
| 64651-7749-1 | Intellishade Original SPF 45 | 1 in 1 CARTON | CREAM | 1 | 13 | |
| 64651-7749-2 | Intellishade Original SPF 45 | 227 g in 1 TUBE | CREAM | 227 | 13 | |
| 64651-7749-3 | Intellishade Original SPF 45 | 3 g in 1 TUBE | CREAM | 3 | 13 |
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.