NDC 70108-119-04 - Smart Care 2 HAND SANITIZERS 1.35 FL OZ (FRENCH VANILLA, CHERRY BLOSSOM)
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
- 70108-119
- Requested NDC
- 70108-119-04
- Package NDCs from labels
- 70108-119-05, 70108-119-04, 70108-119-01, 70108-119-02, 70108-119-03
- Manufacturer
- Ashtel Studios, Inc.
- Effective date
- 2026-07-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Smart Care ® 2 HAND SANITIZERS 1.35 FL OZ (FRENCH VANILLA, CHERRY BLOSSOM) | Ashtel Studios, Inc. | 2026-07-09 | HUMAN OTC DRUG LABEL |
| Ethyl Alcohol - Ashtel Studios, Inc. | Ashtel Studios, Inc. | 2026-05-12 | HUMAN OTC DRUG LABEL |
| Smart Care ® Cherry Blossom HAND SANITIZER SPRAY | Ashtel Studios, Inc. | 2025-09-19 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70108-119-01 | Smart Care Cherry Blossom HAND SANITIZER | 30 mL in 1 BOTTLE, SPRAY | SPRAY | 30 | 3 | |
| 70108-119-02 | Smart Care Cherry Blossom HAND SANITIZER | 30 mL in 1 BOTTLE, SPRAY | SPRAY | 30 | 3 | |
| 70108-119-02 | Smart Care Cherry Blossom HAND SANITIZER | 1 in 1 BOX | SPRAY | 1 | 3 | |
| 70108-119-03 | Smart Care Cherry Blossom HAND SANITIZER | 1 in 1 BOX | SPRAY | 1 | 3 | |
| 70108-119-03 | Smart Care Cherry Blossom HAND SANITIZER | 40 mL in 1 BOTTLE, SPRAY | SPRAY | 40 | 3 | |
| 70108-119-04 | Smart Care 4 HAND SANITIZERS 1.35 FL OZ (CHERRY BLOSSOM, GARDENIA, COCONUT HONEY, LAVENDER VANILLA) | 40 mL in 1 BOTTLE, SPRAY | SPRAY | 40 mL | 70 mL in 100mL | 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.