hand sanitizer
- Product NDC
- 87492-005
- Requested package NDC
- 87492-005-01
- 11-digit product format
- 874920005
- Labeler code
- 87492
- Product ID
- 87492-005_561af497-f33d-550e-e063-6294a90a29de
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- hand sanitizer
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Shenzhen yuehaotong Technology Co., Ltd
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-03-18
- Substance
- ALCOHOL
- Active strength
- 62 mL/100mL
- 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 mL/100mL |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 3K9958V90M | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 561af7a3-25a5-1384-e063-6394a90abb59 | Available on FDA.report |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| hand sanitizer | HAND SANITIZER | Shenzhen yuehaotong Technology Co., Ltd | 561af7a3-25a5-1384-e063-6394a90abb59 | 2026-07-08 | Warnings | 87492-005-01 87492-005 87492000501 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 87492-005-01 | 87492000501 | 1 BOTTLE in 1 BOX (87492-005-01) / 30 mL in 1 BOTTLE | 1 bottle | 2026-03-18 | No | No | Current |