Hand Sanitizer
- Product NDC
- 87269-001
- 11-digit product format
- 872690001
- Labeler code
- 87269
- Product ID
- 87269-001_a7b6474b-d181-39bb-e053-2a95a90ae247
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- hand washing
- Dosage form
- GEL
- Route
- EXTRACORPOREAL
- Labeler
- NINGBO MEIDI COSMETICS CO., LTD.
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-06-10
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 375 mL/500mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 87269-001-01 | Hand Sanitizer | 500 mL in 1 BOTTLE | GEL | 500 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 87269-001 | HAND SANITIZER (HAND WASHING) GEL [NINGBO MEIDI COSMETICS CO., LTD.] | 1 | Legacy NDC, 1 package rows | 20200611_a7b6474b-d180-39bb-e053-2a95a90ae247.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 |
|---|
| 87269-001-01 | 87269000101 | 500 mL in 1 BOTTLE (87269-001-01) | 500 ml | 2020-06-10 | 0000-00-00 | No | No | Current |