Hand Sanitizer
- Product NDC
- 87660-103
- 11-digit product format
- 876600103
- Labeler code
- 87660
- Product ID
- 87660-103_52505999-da20-6273-e063-6294a90a31a3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Guangdong Yanze Biotechnology Co., Ltd.
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-05-18
- Substance
- ALCOHOL
- Active strength
- 6.2 mL/10mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Hand Sanitizer
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | 6.2 mL/10mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 87660-103-01 | Hand Sanitizer | 35 mL in 1 BOTTLE | LIQUID | 35 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87660-103-01 | 87660010301 | 35 mL in 1 BOTTLE (87660-103-01) | 35 ml | 2026-05-18 | No | No | Current |