HAND SANITIZER
- Product NDC
- 75023-004
- 11-digit product format
- 750230004
- Labeler code
- 75023
- Product ID
- 75023-004_aa051c07-043f-470a-e053-2995a90a3b5d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DENATURED DT ETHYL ALCOHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- SUN WAVE WELLNESS, LLC
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-07-05
- 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 |
|---|
| 75023-004-01 | HAND SANITIZER | 100 mL in 1 BOTTLE, SPRAY | LIQUID | 100 | | 1 |
| 75023-004-02 | HAND SANITIZER | 100 mL in 1 BOTTLE, DISPENSING | LIQUID | 100 | | 1 |
| 75023-004-03 | HAND SANITIZER | 100 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 100 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 75023-004 | HAND SANITIZER (DENATURED DT ETHYL ALCOHOL) LIQUID [SUN WAVE WELLNESS, LLC] | 1 | Legacy NDC, 3 package rows | 20200827_aa05201e-d0b7-61c8-e053-2a95a90a0f2f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 75023-004-01 | 75023000401 | 100 mL in 1 BOTTLE, SPRAY (75023-004-01) | 100 ml | 2020-07-05 | 0000-00-00 | No | No | Current |
| 75023-004-02 | 75023000402 | 100 mL in 1 BOTTLE, DISPENSING (75023-004-02) | 100 ml | 2020-07-05 | 0000-00-00 | No | No | Current |
| 75023-004-03 | 75023000403 | 100 mL in 1 BOTTLE, WITH APPLICATOR (75023-004-03) | 100 ml | 2020-07-05 | 0000-00-00 | No | No | Current |