Hand Sanitizer Original
- Product NDC
- 57337-117
- 11-digit product format
- 573370117
- Labeler code
- 57337
- Product ID
- 57337-117_2e0138ca-c555-7125-e063-6394a90adc61
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ethyl Alcohol
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Ningbo Rejoice International
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-03-05
- Substance
- ALCOHOL
- Active strength
- 70 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Hand Sanitizer Original
- Brand name suffix
- 1.8 oz
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | 70 mL/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
| Rxcui | 582753 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 57337-117-01 | Hand Sanitizer Original1.8 oz | 53 mL in 1 BOTTLE | LIQUID | 53 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 57337-117 | HAND SANITIZER ORIGINAL 1.8 OZ (ETHYL ALCOHOL) LIQUID [NINGBO REJOICE INTERNATIONAL] | 2 | Current NDC, Legacy NDC, 1 package rows | 20250215_a26a866a-bb5f-4b5f-e053-2995a90a9745.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 57337-117-01 | 57337011701 | 53 mL in 1 BOTTLE (57337-117-01) | 53 ml | 2020-03-05 | 0000-00-00 | No | No | Current |