Alcohol Free Hand Sanitizer
- Product NDC
- 87001-004
- 11-digit product format
- 870010004
- Labeler code
- 87001
- Product ID
- 87001-004_3c27353a-d762-8c1f-e063-6394a90ae38e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZALKONIUM CHLORIDE
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- HAIAN KANGRUI TEXTILE CO., LTD.
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-08-12
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- .3 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Alcohol Free Hand Sanitizer
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | .3 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F5UM2KM3W7 |
| Rxcui | 2368187 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 87001-004-01 | Alcohol Free Hand Sanitizer | 15 mL in 1 BOTTLE | GEL | 15 | | 1 |
| 87001-004-02 | Alcohol Free Hand Sanitizer | 30 mL in 1 BOTTLE | GEL | 30 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87001-004-01 | 87001000401 | 15 mL in 1 BOTTLE (87001-004-01) | 15 ml | 2025-08-12 | No | No | Historical |
| 87001-004-02 | 87001000402 | 30 mL in 1 BOTTLE (87001-004-02) | 30 ml | 2025-08-12 | No | No | Historical |