NDC 55926-0024-02 - EmuAid
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
- 55926-0024
- Requested NDC
- 55926-0024-02
- Package NDCs from labels
- 55926-0024-2, 55926-0024-02
- Manufacturer
- Speer Laboratories, LLC | Product by O2, Inc.
- Effective date
- 2021-01-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| EmuAid - Speer Laboratories, LLC | Product by O2, Inc. | Speer Laboratories, LLC | Product by O2, Inc. | 2021-01-14 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55926-0024-2 | EmuAid | 59 mL in 1 PACKAGE | OINTMENT | 59 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 55926-0024 | EMUAID (SILVER) OINTMENT [SPEER LABORATORIES, LLC] | 3 | Current NDC, Legacy NDC, 1 package rows | 20210114_07b160d3-107c-4c29-a38e-f343e5b3a714.zip |
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.