Hand Sanitizer
- Product NDC
- 75321-2032
- 11-digit product format
- 753212032
- Labeler code
- 75321
- Product ID
- 75321-2032_aa6b99cc-82e0-3faa-e053-2a95a90afb9f
- 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
- 662 mL/946.35mL
- 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 |
|---|
| 75321-2032-2 | Hand Sanitizer | 946.35 mL in 1 BOTTLE | GEL | 946.35 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 75321-2032 | HAND SANITIZER (ALCOHOL) GEL [SUNBEAM LABORATORIES LLC] | 1 | Legacy NDC, 1 package rows | 20200715_aa6b7373-15a8-1ca4-e053-2a95a90a1786.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 |
|---|
| 75321-2032-2 | 75321203202 | 946.35 mL in 1 BOTTLE (75321-2032-2) | 946.35 ml | 2020-03-30 | 0000-00-00 | No | No | Current |