NDC 64539-005-01 - Cicatrix Skin Protectant
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
- 64539-005
- Requested NDC
- 64539-005-01
- Package NDCs from labels
- 64539-005-01, 64539-005-02
- Manufacturer
- Catalysis, SL
- Effective date
- 2017-06-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Cicatrix Skin Protectant - Catalysis, SL | Catalysis, SL | 2017-06-28 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 64539-005-02 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-b7d9-f424-e053-dadaa90a57ce | Cicatrix |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 64539-005-01 | Cicatrix Skin Protectant | 50 mL in 1 BOTTLE, PUMP | CREAM | 50 | 2 | |
| 64539-005-02 | Cicatrix Skin Protectant | 1 in 1 BOX | CREAM | 1 | 2 |
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.