NDC 80230-007-01 - Hand Sanitizer Single Use
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
- 80230-007
- Requested NDC
- 80230-007-01
- Package NDCs from labels
- 80230-007-01, 80230-007-02, 80230-007-08, 80230-007-16
- Manufacturer
- Skymall Holdings LLC
- Effective date
- 2020-09-16
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Hand Sanitizer Single Use - Skymall Holdings LLC | Skymall Holdings LLC | 2020-09-16 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 80230-007-02 | 2022-07-29 | C162847 | 48780-1 | e4f33bdf-a3ee-d8a0-e053-dadaa90a6e4e | Skymall Zink Brntag Crayola Rhinestone Clrless Paks Sanitizer Gel Alc75 |
| 80230-007-08 | 2022-07-29 | C162847 | 48780-1 | e4f33bdf-a3ee-d8a0-e053-dadaa90a6e4e | Skymall Zink Brntag Crayola Rhinestone Clrless Paks Sanitizer Gel Alc75 |
| 80230-007-16 | 2022-07-29 | C162847 | 48780-1 | e4f33bdf-a3ee-d8a0-e053-dadaa90a6e4e | Skymall Zink Brntag Crayola Rhinestone Clrless Paks Sanitizer Gel Alc75 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 80230-007-01 | Hand SanitizerSingle Use | 2 mL in 1 PACKET | GEL | 2 | 2 | |
| 80230-007-02 | Hand SanitizerSingle Use | 100 in 1 BOX | GEL | 100 | 2 | |
| 80230-007-08 | Hand SanitizerSingle Use | 236 mL in 1 BOTTLE, PUMP | GEL | 236 | 2 | |
| 80230-007-16 | Hand SanitizerSingle Use | 499 mL in 1 BOTTLE, PUMP | GEL | 499 | 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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.