Hand Sanitizer
- Product NDC
- 74458-968
- Requested package NDC
- 74458-968-01
- 11-digit product format
- 744580968
- Labeler code
- 74458
- Product ID
- 74458-968_5d93c5c5-c03c-63c7-e063-6294a90a1049
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ETHYL ALCOHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Guangzhou Yilong Cosmetics.,Ltd
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-10-10
- Substance
- ALCOHOL
- Active strength
- 62 g/100mg
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Hand Sanitizer
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ALCOHOL | 62 g/100mg |
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.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 74458-968-01 | 74458096801 | 35 mg in 1 BOTTLE (74458-968-01) | 35 mg | 2026-10-10 | No | No | Current |