NDC 69579-102-01 - P1P Chitosan V-mask
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
- 69579-102
- Requested NDC
- 69579-102-01
- Package NDCs from labels
- 69579-102-01, 69579-102-02
- Manufacturer
- Phytos Co., Ltd.
- Effective date
- 2015-01-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| P1P & Chitosan V-mask | Phytos Co., Ltd. | 2015-01-28 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 69579-102-02 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-dd14-f424-e053-dadaa90a57ce | P1P & Chitosan V-mask |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69579-102-01 | P1P Chitosan V-mask | 25 mL in 1 PATCH | PATCH | 25 | 2 | |
| 69579-102-02 | P1P Chitosan V-mask | 5 in 1 BOX | PATCH | 5 | 2 |
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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| Sunscreen SPF 50 | SUNSCREEN SPF 50 | Guangzhou Ariel Biotech Co., Ltd. | 4dd1b722-4448-9675-e063-6294a90a5f4f | 2026-03-24 | Warnings | 25X51I8RD4 YSE9PPT4TH |
| Sterile Water | WATER | Hospira, Inc. | 2b9ea23a-f9e9-48a8-25b7-519e3bbd6828 | 2026-03-18 | Warnings, Adverse reactions | 059QF0KO0R |
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| TINTED SUNSCREEN FOUNDATION | TINTED SUNSCREEN FOUNDATION | Guanghzou AiXin Biotech Co Ltd | 396393c4-b50c-3877-e063-6294a90a0e9b | 2026-03-17 | Warnings | 059QF0KO0R |
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| Optimel Manuka Forte Eye Gel | GLYCERIN | Melcare Biomedical Pty Ltd | 8e0ed6e8-51fc-7c5b-e053-2a95a90a35a9 | 2026-03-11 | Warnings | PDC6A3C0OX |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.