Hand Sanitizer
- Product NDC
- 87660-106
- 11-digit product format
- 876600106
- Labeler code
- 87660
- Product ID
- 87660-106_5bf5226d-5be3-69af-e063-6294a90a5f78
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol
- Dosage form
- LIQUID
- Route
- CUTANEOUS
- Labeler
- Guangdong Yanze Biotechnology Co., Ltd.
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-06-11
- 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 |
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 |
|---|---|---|---|---|---|---|---|
| 87660-106-01 | 87660010601 | 35 mL in 1 BOTTLE (87660-106-01) | 35 ml | 2026-06-11 | No | No | Current |