Hand Sanitizer
- Product NDC
- 79838-001
- 11-digit product format
- 798380001
- Labeler code
- 79838
- Product ID
- 79838-001_aa92817d-2e6e-242e-e053-2a95a90abcb3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- INTERNATIONAL HARBOR, 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 79838-001-01 | Hand Sanitizer | 1000 mL in 1 BOTTLE | GEL | 1000 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 79838-001 | HAND SANITIZER (ALCOHOL) GEL [INTERNATIONAL HARBOR, LLC] | 1 | Legacy NDC, 1 package rows | 20200804_aa928979-2e9e-270d-e053-2995a90af6ca.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 |
|---|
| 79838-001-01 | 79838000101 | 1000 mL in 1 BOTTLE (79838-001-01) | 1000 ml | 2020-03-30 | 0000-00-00 | No | No | Current |