Hand Sanitizer
- Product NDC
- 73939-401
- 11-digit product format
- 739390401
- Labeler code
- 73939
- Product ID
- 73939-401_a475d89c-0416-d50b-e053-2995a90a83b5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- DISTILLERS WAY LLC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-03-30
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 80 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73939-401-05 | Hand Sanitizer | 500 mL in 1 BOTTLE, PLASTIC | LIQUID | 500 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73939-401 | HAND SANITIZER (ALCOHOL) LIQUID [DISTILLERS WAY LLC] | 2 | Legacy NDC, 1 package rows | 20200430_a21b8643-6f34-4e0c-e053-2a95a90a226a.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 |
|---|
| 73939-401-05 | 73939040105 | 500 mL in 1 BOTTLE, PLASTIC (73939-401-05) | 500 ml | 2020-04-30 | 0000-00-00 | No | No | Current |