Hand Sanitizer Gel
- Product NDC
- 75321-2002
- 11-digit product format
- 753212002
- Labeler code
- 75321
- Product ID
- 75321-2002_aa67041e-bed2-3217-e053-2995a90ab321
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- SunBeam Laboratories LLC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-03-30
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 41 mL/59.15mL
- 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 |
|---|
| 75321-2002-2 | Hand Sanitizer Gel | 59.15 mL in 1 BOTTLE | GEL | 59.15 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 75321-2002 | HAND SANITIZER GEL (ALCOHOL) GEL [SUNBEAM LABORATORIES LLC] | 1 | Legacy NDC, 1 package rows | 20200715_aa6736ab-7bd9-1bfa-e053-2a95a90a2f2c.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 |
|---|
| 75321-2002-2 | 75321200202 | 59.15 mL in 1 BOTTLE (75321-2002-2) | 59.15 ml | 2020-03-30 | 0000-00-00 | No | No | Current |