NDC 68828-243 - Royal Jelly Kit Jafra
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
- 68828-243
- Package NDCs from labels
- 68828-243-01
- Manufacturer
- JAFRA COSMETICS INTERNATIONAL | Jafra Manufacturing, S.A. de C.V.
- Effective date
- 2020-06-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Jafra Royal Jelly Kit | JAFRA COSMETICS INTERNATIONAL | Jafra Manufacturing, S.A. de C.V. | 2020-06-22 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68828-243-01 | Royal Jelly KitJafra | 15 mL in 1 BOTTLE | CREAM | 15 mL | 7 g in 100mL | 4 |
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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| Neutrogena Ultra Sheer Body Mist Sunscreen Broad Spectrum SPF 70 | AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE | Kenvue Brands LLC | 97795f0e-d867-4e17-b7c9-ede08e7df70c | 2025-09-12 | Warnings | 5A68WGF6WM V06SV4M95S G63QQF2NOX 4X49Y0596W |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.