Onyx Advanced Hand Sanitizer
- Product NDC
- 75403-000
- 11-digit product format
- 754030000
- Labeler code
- 75403
- Product ID
- 75403-000_a3d7426f-58a0-0eed-e053-2995a90a03b0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- ONYX PREMIERE LLC
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-04-01
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 1 mL/mL
- 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 |
|---|
| 75403-000-01 | Onyx Advanced Hand Sanitizer | 250 mL in 1 POUCH | GEL | 250 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 75403-000 | ONYX ADVANCED HAND SANITIZER (ALCOHOL) GEL [ONYX PREMIERE LLC] | 1 | Legacy NDC, 1 package rows | 20200422_a3d73e4f-893e-6668-e053-2a95a90a6592.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 |
|---|
| 75403-000-01 | 75403000001 | 250 mL in 1 POUCH (75403-000-01) | 250 ml | 2020-04-01 | 0000-00-00 | No | No | Current |