NDC 76383-014-07 - Hand Sanitizer with Vitamin E
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
- 76383-014
- Requested NDC
- 76383-014-07
- Package NDCs from labels
- 76383-014-01, 76383-014-03, 76383-014-08, 76383-014-12, 76383-014-30, 76383-014-34, 76383-014-28, 76383-014-02, 76383-014-16, 76383-014-07, 76383-014-50
- Manufacturer
- BBC GROUP LIMITED
- Effective date
- 2020-09-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Hand Sanitizer with Vitamin E - BBC GROUP LIMITED | BBC GROUP LIMITED | 2020-09-11 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 76383-014-01 | Hand Sanitizerwith Vitamin E | 50 mL in 1 BOTTLE, PLASTIC | LIQUID | 50 | 4 | |
| 76383-014-02 | Hand Sanitizerwith Vitamin E | 30 mL in 1 BOTTLE, PLASTIC | LIQUID | 30 | 4 | |
| 76383-014-03 | Hand Sanitizerwith Vitamin E | 89 mL in 1 BOTTLE, PLASTIC | LIQUID | 89 | 4 | |
| 76383-014-07 | Hand Sanitizerwith Vitamin E | 2 mL in 1 PACKET | LIQUID | 2 | 4 | |
| 76383-014-08 | Hand Sanitizerwith Vitamin E | 236 mL in 1 BOTTLE, PLASTIC | LIQUID | 236 | 4 | |
| 76383-014-12 | Hand Sanitizerwith Vitamin E | 354 mL in 1 BOTTLE, PUMP | LIQUID | 354 | 4 | |
| 76383-014-16 | Hand Sanitizerwith Vitamin E | 473 mL in 1 BOTTLE, PLASTIC | LIQUID | 473 | 4 | |
| 76383-014-28 | Hand Sanitizerwith Vitamin E | 3789 mL in 1 BOTTLE, PLASTIC | LIQUID | 3789 | 4 | |
| 76383-014-30 | Hand Sanitizerwith Vitamin E | 887 mL in 1 BOTTLE, PUMP | LIQUID | 887 | 4 | |
| 76383-014-34 | Hand Sanitizerwith Vitamin E | 1000 mL in 1 BOTTLE, PUMP | LIQUID | 1000 | 4 | |
| 76383-014-50 | Hand Sanitizerwith Vitamin E | 50 in 1 BOX | LIQUID | 50 | 4 |
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.