NDC 68828-501 - Jafra Royal Jelly Revitalize
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
- 68828-501
- Package NDCs from labels
- 68828-501-01, 68828-501-02
- Manufacturer
- JAFRA COSMETICS INTERNATIONAL | Jafra Manufacturing, S.A. de C.V
- Effective date
- 2018-04-20
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| AVOBENZONE - JAFRA COSMETICS INTERNATIONAL | Jafra Manufacturing, S.A. de C.V | JAFRA COSMETICS INTERNATIONAL | Jafra Manufacturing, S.A. de C.V | 2018-04-20 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68828-501-01 | Jafra Royal Jelly Revitalize | 14 mL in 1 TUBE | LOTION | 14 mL | 7 g in 100mL | 1 |
| 68828-501-02 | Jafra Royal Jelly Revitalize | 7.5 mL in 1 PACKAGE | LOTION | 14 mL | 3 g in 100mL | 1 |
DailyMed Dashboard NDC Coverage#
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.