NDC 78035-001-01 - rareESSENCE Hand Sanitizer
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
- 78035-001
- Requested NDC
- 78035-001-01
- Package NDCs from labels
- 78035-001-01, 78035-001-02, 78035-001-03, 78035-001-04, 78035-001-05, 78035-001-06
- Manufacturer
- rareESSENCE, LLC | Diversified Manufacturing Corporation
- Effective date
- 2020-06-02
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ethyl Alcohol - rareESSENCE, LLC | Diversified Manufacturing Corporation | rareESSENCE, LLC | Diversified Manufacturing Corporation | 2020-06-02 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 78035-001-03 | 2023-01-30 | C162847 | 48780-1 | f386c649-a5cf-0266-e053-dadaa90a7c1a | Drug Facts |
| 78035-001-06 | 2023-01-30 | C162847 | 48780-1 | f386c649-a5cf-0266-e053-dadaa90a7c1a | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 78035-001-01 | rareESSENCE Hand Sanitizer | 59 mL in 1 BOTTLE, SPRAY | LIQUID | 59 | 1 | |
| 78035-001-02 | rareESSENCE Hand Sanitizer | 12 in 1 CASE | LIQUID | 12 | 1 | |
| 78035-001-03 | rareESSENCE Hand Sanitizer | 48 in 1 CARTON | LIQUID | 48 | 1 | |
| 78035-001-04 | rareESSENCE Hand Sanitizer | 118 mL in 1 BOTTLE, SPRAY | LIQUID | 118 | 1 | |
| 78035-001-05 | rareESSENCE Hand Sanitizer | 12 in 1 CASE | LIQUID | 12 | 1 | |
| 78035-001-06 | rareESSENCE Hand Sanitizer | 48 in 1 CARTON | LIQUID | 48 | 1 |
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.