NDC 69579-104-01 - P1P Magic Whitening Antiaging
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
- 69579-104
- Requested NDC
- 69579-104-01
- Package NDCs from labels
- 69579-104-01, 69579-104-02
- Manufacturer
- Phytos Co., Ltd.
- Effective date
- 2015-02-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| P1P Magic Whitening & Antiaging | Phytos Co., Ltd. | 2015-02-18 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 69579-104-02 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-0184-f424-e053-dadaa90a57ce | P1P Magic Whitening & Antiaging |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69579-104-01 | P1P Magic Whitening Antiaging | 5 mL in 1 AMPULE | LIQUID | 5 | 1 | |
| 69579-104-02 | P1P Magic Whitening Antiaging | 5 in 1 CARTON | LIQUID | 5 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
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.