Hand Sanitizer
- Product NDC
- 41366-017
- 11-digit product format
- 413660017
- Labeler code
- 41366
- Product ID
- 41366-017_454588b7-63fd-bf46-e063-6394a90adb4d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Hand Sanitizer
- Dosage form
- GEL
- Route
- EXTRACORPOREAL
- Labeler
- Zhejiang Meimi Technology Co., Ltd.
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-04-05
- 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
- 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 | 581662 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 41366-017-01 | Hand Sanitizer | 89 mL in 1 BOTTLE | GEL | 89 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41366-017 | HAND SANITIZER GEL [ZHEJIANG MEIMI TECHNOLOGY CO., LTD.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20240121_bf399508-bd29-0d90-e053-2995a90a067f.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 |
|---|
| 41366-017-01 | 41366001701 | 89 mL in 1 BOTTLE (41366-017-01) | 89 ml | 2021-04-05 | 0000-00-00 | No | No | Current |