Hand Sanitizer
- Product NDC
- 74418-202
- 11-digit product format
- 744180202
- Labeler code
- 74418
- Product ID
- 74418-202_a46c6569-a864-6b57-e053-2995a90a7951
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ETHYL ALCOHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Medustry LLC
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-04-24
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 75 mL/100mL
- 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 |
|---|
| 74418-202-01 | Hand Sanitizer | 59 mL in 1 BOTTLE | GEL | 59 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 74418-202 | HAND SANITIZER (ETHYL ALCOHOL) GEL [MEDUSTRY LLC] | 1 | Legacy NDC, 1 package rows | 20200430_a46c6569-a863-6b57-e053-2995a90a7951.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 |
|---|
| 74418-202-01 | 74418020201 | 59 mL in 1 BOTTLE (74418-202-01) | 59 ml | 2020-04-24 | 0000-00-00 | No | No | Current |