Instant Hand Sanitizer
- Product NDC
- 52923-002
- 11-digit product format
- 529230002
- Labeler code
- 52923
- Product ID
- 52923-002_a62082db-7291-c9e5-e053-2a95a90a6620
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Instant Hand Sanitizer
- Dosage form
- GEL
- Route
- EXTRACORPOREAL
- Labeler
- ADF HI-TECH DISINFECTANTS CO., LTD.
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-05-19
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 351 mL/502mL
- 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 |
|---|
| 52923-002-01 | Instant Hand Sanitizer | 502 mL in 1 BOTTLE | GEL | 502 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52923-002 | INSTANT HAND SANITIZER GEL [ADF HI-TECH DISINFECTANTS CO., LTD.] | 1 | Legacy NDC, 1 package rows | 20200521_a62082b5-4bfd-7939-e053-2995a90a75c7.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52923-002-01 | 52923000201 | 502 mL in 1 BOTTLE (52923-002-01) | 502 ml | 2020-05-19 | 0000-00-00 | No | No | Current |