Hand Sanitizer
- Product NDC
- 52578-002
- 11-digit product format
- 525780002
- Labeler code
- 52578
- Product ID
- 52578-002_a6846fae-bb6c-7bf9-e053-2995a90ac57f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Hand Sanitizer
- Dosage form
- LIQUID
- Route
- EXTRACORPOREAL
- Labeler
- FUJIAN BLUE-TOUCH PRODUCTS INC.
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-05-11
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 48 mL/68mL
- 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 |
|---|
| 52578-002-01 | Hand Sanitizer | 68 mL in 1 BOTTLE | LIQUID | 68 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52578-002 | HAND SANITIZER LIQUID [FUJIAN BLUE-TOUCH PRODUCTS INC.] | 2 | Legacy NDC, 1 package rows | 20200527_a55c5d9e-ab38-4b30-e053-2995a90a57e6.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 |
|---|
| 52578-002-01 | 52578000201 | 68 mL in 1 BOTTLE (52578-002-01) | 68 ml | 2020-05-11 | 0000-00-00 | No | No | Current |