QUEEN MAX
- Product NDC
- 78141-123
- 11-digit product format
- 781410123
- Labeler code
- 78141
- Product ID
- 78141-123_a64d3577-912b-7e77-e053-2a95a90aca96
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Hand Sanitizer
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Fuson LLC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-05-25
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 75 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 |
|---|
| 78141-123-10 | QUEEN MAX | 100 mL in 1 BOTTLE | LIQUID | 100 | | 1 |
| 78141-123-25 | QUEEN MAX | 25 mL in 1 BOTTLE | LIQUID | 25 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 78141-123 | QUEEN MAX (HAND SANITIZER) LIQUID [FUSON LLC] | 1 | Legacy NDC, 2 package rows | 20200525_a64d3577-9139-7e77-e053-2a95a90aca96.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 |
|---|
| 78141-123-10 | 78141012310 | 100 mL in 1 BOTTLE (78141-123-10) | 100 ml | 2020-05-25 | 0000-00-00 | No | No | Current |
| 78141-123-25 | 78141012325 | 25 mL in 1 BOTTLE (78141-123-25) | 25 ml | 2020-05-25 | 0000-00-00 | No | No | Current |