UZO Hand Sanitizer
- Product NDC
- 79740-005
- 11-digit product format
- 797400005
- Labeler code
- 79740
- Product ID
- 79740-005_b1c099fb-64ee-c252-e053-2a95a90a8c11
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Hand Sanitizer
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- ANTHOS GROUP, INC, THE
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-03-30
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 70 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 |
|---|
| 79740-005-01 | UZO Hand Sanitizer | 240 mL in 1 BOTTLE | LIQUID | 240 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 79740-005 | UZO HAND SANITIZER (HAND SANITIZER) LIQUID [ANTHOS GROUP, INC, THE] | 2 | Legacy NDC, 1 package rows | 20240221_b1c0a0d3-790a-3c04-e053-2995a90aadb4.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 |
|---|
| 79740-005-01 | 79740000501 | 240 mL in 1 BOTTLE (79740-005-01) | 240 ml | 2020-03-30 | 0000-00-00 | No | No | Current |